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6505-01-280-2318

20 Products

PIPRACIL

PIPERACILLIN SODIUM,USP

NSN, MFG P/N

6505012802318

NSN

6505-01-280-2318

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PIPRACIL

PIPERACILLIN SODIUM,USP

NSN, MFG P/N

6505012802318

NSN

6505-01-280-2318

MFG

AMERICAN CYANAMID CO LEDERLE LABORATORIES DIV

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 4.000 GRAMS PIPERACILLIN EQUIVALENT
ADMINISTRATION: INTRAMUSCULAR OR INTRAVENOUS
III PART NAME ASSIGNED BY CONTROLLING AGENCY: PIPERACILLIN SODIUM STERILE USP 4GM POWDER INTRAMUSCLAR/IV VIAL 10S
PHYSICAL FORM: POWDER
PRIMARY CONTAINER CONTENT QUANTITY: 4.000 GRAMS OF ACTIVE INGREDIENT
PRIMARY CONTAINER TYPE: VIAL
TOTAL PRIMARY CONTAINER QUANTITY: 10

7651-03

HEPARIN SODIUM INJECTION,USP

NSN, MFG P/N

6505012799610

NSN

6505-01-279-9610

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7651-03

HEPARIN SODIUM INJECTION,USP

NSN, MFG P/N

6505012799610

NSN

6505-01-279-9610

MFG

ABBOTT LABORATORIES INC. DIV HOSPITAL PRODUCTS DIVISION

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 50.000 UNITS HEPARIN SODIUM PER MILLILITER
ADMINISTRATION: INTRAVENOUS
FEATURES PROVIDED: STERILE
PHARMACEUTICAL VEHICLE TYPE: AQUEOUS
PRIMARY CONTAINER CONTENT QUANTITY: 500.000 MILLILITERS
PRIMARY CONTAINER TYPE: BAG, PLASTIC
RAW MATERIAL SOURCE: PORCINE INTESTINAL MUCOSA
SPECIAL FEATURES: NONPYROGENIC

NDC00074-7651-03

HEPARIN SODIUM INJECTION,USP

NSN, MFG P/N

6505012799610

NSN

6505-01-279-9610

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NDC00074-7651-03

HEPARIN SODIUM INJECTION,USP

NSN, MFG P/N

6505012799610

NSN

6505-01-279-9610

MFG

ABBOTT LABORATORIES INC. DIV HOSPITAL PRODUCTS DIVISION

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 50.000 UNITS HEPARIN SODIUM PER MILLILITER
ADMINISTRATION: INTRAVENOUS
FEATURES PROVIDED: STERILE
PHARMACEUTICAL VEHICLE TYPE: AQUEOUS
PRIMARY CONTAINER CONTENT QUANTITY: 500.000 MILLILITERS
PRIMARY CONTAINER TYPE: BAG, PLASTIC
RAW MATERIAL SOURCE: PORCINE INTESTINAL MUCOSA
SPECIAL FEATURES: NONPYROGENIC

METRODIN

UROFOLLITROPIN FOR INJECTION

NSN, MFG P/N

6505012799623

NSN

6505-01-279-9623

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METRODIN

UROFOLLITROPIN FOR INJECTION

NSN, MFG P/N

6505012799623

NSN

6505-01-279-9623

MFG

SERONO-BAKER DIAGNOSTICS INC

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 75.000 INTERNATIONAL UNITS FOLLICLE-STIMULATING HORMONE ACTIVITY EQUIVALENT
ADMINISTRATION: INTRAMUSCULAR
FEATURES PROVIDED: STERILE
III PART NAME ASSIGNED BY CONTROLLING AGENCY: UROFOLLITROPIN FOR INJECTION FREEZE-DRIED POWDER 75 I.U. AMPUL
PHYSICAL FORM: FREEZE-DRIED POWDER OR PELLET,STERILE
PRIMARY CONTAINER CONTENT QUANTITY: 75.000 INTERNATIONAL UNITS OF ACTIVE INGREDIENT
PRIMARY CONTAINER TYPE: AMPUL
SPECIAL FEATURES: WITH ONE 2 ML AMPUL OF SODIUM CHLORIDE INJECTION,USP

NDC44087-6075-01

UROFOLLITROPIN FOR INJECTION

NSN, MFG P/N

6505012799623

NSN

6505-01-279-9623

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NDC44087-6075-01

UROFOLLITROPIN FOR INJECTION

NSN, MFG P/N

6505012799623

NSN

6505-01-279-9623

MFG

SERONO-BAKER DIAGNOSTICS INC

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 75.000 INTERNATIONAL UNITS FOLLICLE-STIMULATING HORMONE ACTIVITY EQUIVALENT
ADMINISTRATION: INTRAMUSCULAR
FEATURES PROVIDED: STERILE
III PART NAME ASSIGNED BY CONTROLLING AGENCY: UROFOLLITROPIN FOR INJECTION FREEZE-DRIED POWDER 75 I.U. AMPUL
PHYSICAL FORM: FREEZE-DRIED POWDER OR PELLET,STERILE
PRIMARY CONTAINER CONTENT QUANTITY: 75.000 INTERNATIONAL UNITS OF ACTIVE INGREDIENT
PRIMARY CONTAINER TYPE: AMPUL
SPECIAL FEATURES: WITH ONE 2 ML AMPUL OF SODIUM CHLORIDE INJECTION,USP

NDC44087-7075-03

UROFOLLITROPIN FOR INJECTION

NSN, MFG P/N

6505012799623

NSN

6505-01-279-9623

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NDC44087-7075-03

UROFOLLITROPIN FOR INJECTION

NSN, MFG P/N

6505012799623

NSN

6505-01-279-9623

MFG

SERONO-BAKER DIAGNOSTICS INC

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 75.000 INTERNATIONAL UNITS FOLLICLE-STIMULATING HORMONE ACTIVITY EQUIVALENT
ADMINISTRATION: INTRAMUSCULAR
FEATURES PROVIDED: STERILE
III PART NAME ASSIGNED BY CONTROLLING AGENCY: UROFOLLITROPIN FOR INJECTION FREEZE-DRIED POWDER 75 I.U. AMPUL
PHYSICAL FORM: FREEZE-DRIED POWDER OR PELLET,STERILE
PRIMARY CONTAINER CONTENT QUANTITY: 75.000 INTERNATIONAL UNITS OF ACTIVE INGREDIENT
PRIMARY CONTAINER TYPE: AMPUL
SPECIAL FEATURES: WITH ONE 2 ML AMPUL OF SODIUM CHLORIDE INJECTION,USP

NDC54569-4528-00

UROFOLLITROPIN FOR INJECTION

NSN, MFG P/N

6505012799623

NSN

6505-01-279-9623

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NDC54569-4528-00

UROFOLLITROPIN FOR INJECTION

NSN, MFG P/N

6505012799623

NSN

6505-01-279-9623

MFG

MERCK SHARP & DOHME CORP. D IV CORPORATE HEADQUARTERS

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 75.000 INTERNATIONAL UNITS FOLLICLE-STIMULATING HORMONE ACTIVITY EQUIVALENT
ADMINISTRATION: INTRAMUSCULAR
FEATURES PROVIDED: STERILE
III PART NAME ASSIGNED BY CONTROLLING AGENCY: UROFOLLITROPIN FOR INJECTION FREEZE-DRIED POWDER 75 I.U. AMPUL
PHYSICAL FORM: FREEZE-DRIED POWDER OR PELLET,STERILE
PRIMARY CONTAINER CONTENT QUANTITY: 75.000 INTERNATIONAL UNITS OF ACTIVE INGREDIENT
PRIMARY CONTAINER TYPE: AMPUL
SPECIAL FEATURES: WITH ONE 2 ML AMPUL OF SODIUM CHLORIDE INJECTION,USP

NDC00006-3552-59

IMIPENEM AND CILASTATIN FOR INJECTION,USP

NSN, MFG P/N

6505012799627

NSN

6505-01-279-9627

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NDC00006-3552-59

IMIPENEM AND CILASTATIN FOR INJECTION,USP

NSN, MFG P/N

6505012799627

NSN

6505-01-279-9627

MFG

MERCK SHARP & DOHME CORP. DBA MERCK DIV US HUMAN HEALTH

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 500.000 MILLIGRAMS CILASTATIN EQUIVALENT AND 500.000 MILLIGRAMS IMIPENEM EQUIVALENT
III PART NAME ASSIGNED BY CONTROLLING AGENCY: IMIPENEM & CILASTATIN SOD F/INJ SGL DOSE FI 1000MG 25S
PHYSICAL FORM: POWDER
PRIMARY CONTAINER CONTENT QUANTITY: 1000.000 MILLIGRAMS OF ACTIVE INGREDIENT
PRIMARY CONTAINER TYPE: VIAL, SINGLE DOSE
SPECIAL FEATURES: 15 ML CAPACITY GLASS VIAL SHALL HAVE A DOUBLE LEAD SCREW THREAD DESIGNED TO INTERLOCK WITH THE INLET PORT OF THE FOLLOWING DILUENT CONTAINERS: 6505-01-260-1237,6505-01-260-1238,6505-01-260-1239,6505-01-260-1241,6505-01-260-1242; THE ASSEMBLY OF THE DRUG
TOTAL PRIMARY CONTAINER QUANTITY: 25
~1: VIAL AND DILUENT CONTAINER SHALL PROVIDE A TAMPER-RESISTANT,STERILE,LEAK PROOF BARRIER; EACH DRUG VIAL SHALL BE ENCLOSED IN AN UPPER AND LOWER PLASTIC SHROUD; THE UPPER SHROUD SHALL BE A STERILITY BARRIER WITH A PULL RING TO ALLOW EASE OF OPENING; THE
~2: LOWER SHROUD SHALL PROVIDE AN INTEGRAL HANGER TO SUPPORT THE ASSEMBLY AND ADMINISTRATION SET; THE VIAL SHALL HAVE A VIEWING PORT TO ALLOW CONFIRMATION OF DRUG ADDITION AND DISSOLUTION

PRIMAXIN

IMIPENEM AND CILASTATIN FOR INJECTION,USP

NSN, MFG P/N

6505012799627

NSN

6505-01-279-9627

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PRIMAXIN

IMIPENEM AND CILASTATIN FOR INJECTION,USP

NSN, MFG P/N

6505012799627

NSN

6505-01-279-9627

MFG

MERCK SHARP & DOHME CORP. DBA MERCK DIV US HUMAN HEALTH

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 500.000 MILLIGRAMS CILASTATIN EQUIVALENT AND 500.000 MILLIGRAMS IMIPENEM EQUIVALENT
III PART NAME ASSIGNED BY CONTROLLING AGENCY: IMIPENEM & CILASTATIN SOD F/INJ SGL DOSE FI 1000MG 25S
PHYSICAL FORM: POWDER
PRIMARY CONTAINER CONTENT QUANTITY: 1000.000 MILLIGRAMS OF ACTIVE INGREDIENT
PRIMARY CONTAINER TYPE: VIAL, SINGLE DOSE
SPECIAL FEATURES: 15 ML CAPACITY GLASS VIAL SHALL HAVE A DOUBLE LEAD SCREW THREAD DESIGNED TO INTERLOCK WITH THE INLET PORT OF THE FOLLOWING DILUENT CONTAINERS: 6505-01-260-1237,6505-01-260-1238,6505-01-260-1239,6505-01-260-1241,6505-01-260-1242; THE ASSEMBLY OF THE DRUG
TOTAL PRIMARY CONTAINER QUANTITY: 25
~1: VIAL AND DILUENT CONTAINER SHALL PROVIDE A TAMPER-RESISTANT,STERILE,LEAK PROOF BARRIER; EACH DRUG VIAL SHALL BE ENCLOSED IN AN UPPER AND LOWER PLASTIC SHROUD; THE UPPER SHROUD SHALL BE A STERILITY BARRIER WITH A PULL RING TO ALLOW EASE OF OPENING; THE
~2: LOWER SHROUD SHALL PROVIDE AN INTEGRAL HANGER TO SUPPORT THE ASSEMBLY AND ADMINISTRATION SET; THE VIAL SHALL HAVE A VIEWING PORT TO ALLOW CONFIRMATION OF DRUG ADDITION AND DISSOLUTION

01420

GENTAMICIN SULFATE INJECTION,USP

NSN, MFG P/N

6505012800050

NSN

6505-01-280-0050

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01420

GENTAMICIN SULFATE INJECTION,USP

NSN, MFG P/N

6505012800050

NSN

6505-01-280-0050

MFG

SOLOPAK MEDICAL PRODUCTS INC

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 40.000 MILLIGRAMS GENTAMICIN SULFATE PER MILLILITER
ADMINISTRATION: INTRAMUSCULAR
PRIMARY CONTAINER CONTENT QUANTITY: 20.000 MILLILITERS
PRIMARY CONTAINER TYPE: VIAL, MULTIPLE DOSE
TOTAL PRIMARY CONTAINER QUANTITY: 25

NDC39769-0014-20

GENTAMICIN SULFATE INJECTION,USP

NSN, MFG P/N

6505012800050

NSN

6505-01-280-0050

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NDC39769-0014-20

GENTAMICIN SULFATE INJECTION,USP

NSN, MFG P/N

6505012800050

NSN

6505-01-280-0050

MFG

SOLOPAK MEDICAL PRODUCTS INC

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 40.000 MILLIGRAMS GENTAMICIN SULFATE PER MILLILITER
ADMINISTRATION: INTRAMUSCULAR
PRIMARY CONTAINER CONTENT QUANTITY: 20.000 MILLILITERS
PRIMARY CONTAINER TYPE: VIAL, MULTIPLE DOSE
TOTAL PRIMARY CONTAINER QUANTITY: 25

NDC00004-1998-06

MIDAZOLAM HYDROCHLORIDE INJECTION

NSN, MFG P/N

6505012801074

NSN

6505-01-280-1074

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NDC00004-1998-06

MIDAZOLAM HYDROCHLORIDE INJECTION

NSN, MFG P/N

6505012801074

NSN

6505-01-280-1074

MFG

HOFFMANN-LA ROCHE INC.

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 1.000 MILLIGRAM MIDAZOLAM EQUIVALENT PER MILLILITER
ADMINISTRATION: INTRAMUSCULAR OR INTRAVENOUS
FEATURES PROVIDED: STERILE
III CONTROLLED SUBSTANCE CLASSIFICATION: SCHEDULE IV
III PART NAME ASSIGNED BY CONTROLLING AGENCY: MIDAZOLAM HYDROCHLORIDE INJECTION 1MG EQUIV PER ML IV 2ML VIAL 10S
III PROTECTIVE STORAGE FEATURE: SECURITY STORAGE
PRIMARY CONTAINER CONTENT QUANTITY: 2.000 MILLILITERS
PRIMARY CONTAINER TYPE: VIAL
TOTAL PRIMARY CONTAINER QUANTITY: 10

NDC00074-2587-02

MIDAZOLAM HYDROCHLORIDE INJECTION

NSN, MFG P/N

6505012801074

NSN

6505-01-280-1074

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NDC00074-2587-02

MIDAZOLAM HYDROCHLORIDE INJECTION

NSN, MFG P/N

6505012801074

NSN

6505-01-280-1074

MFG

ABBOTT LABORATORIES INC. DIV HOSPITAL PRODUCTS DIVISION

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 1.000 MILLIGRAM MIDAZOLAM EQUIVALENT PER MILLILITER
ADMINISTRATION: INTRAMUSCULAR OR INTRAVENOUS
FEATURES PROVIDED: STERILE
III CONTROLLED SUBSTANCE CLASSIFICATION: SCHEDULE IV
III PART NAME ASSIGNED BY CONTROLLING AGENCY: MIDAZOLAM HYDROCHLORIDE INJECTION 1MG EQUIV PER ML IV 2ML VIAL 10S
III PROTECTIVE STORAGE FEATURE: SECURITY STORAGE
PRIMARY CONTAINER CONTENT QUANTITY: 2.000 MILLILITERS
PRIMARY CONTAINER TYPE: VIAL
TOTAL PRIMARY CONTAINER QUANTITY: 10

NDC55390-0137-02

MIDAZOLAM HYDROCHLORIDE INJECTION

NSN, MFG P/N

6505012801074

NSN

6505-01-280-1074

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NDC55390-0137-02

MIDAZOLAM HYDROCHLORIDE INJECTION

NSN, MFG P/N

6505012801074

NSN

6505-01-280-1074

MFG

BEN VENUE LABORATORIES INC DBA BEDFORD LABORATORIES

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 1.000 MILLIGRAM MIDAZOLAM EQUIVALENT PER MILLILITER
ADMINISTRATION: INTRAMUSCULAR OR INTRAVENOUS
FEATURES PROVIDED: STERILE
III CONTROLLED SUBSTANCE CLASSIFICATION: SCHEDULE IV
III PART NAME ASSIGNED BY CONTROLLING AGENCY: MIDAZOLAM HYDROCHLORIDE INJECTION 1MG EQUIV PER ML IV 2ML VIAL 10S
III PROTECTIVE STORAGE FEATURE: SECURITY STORAGE
PRIMARY CONTAINER CONTENT QUANTITY: 2.000 MILLILITERS
PRIMARY CONTAINER TYPE: VIAL
TOTAL PRIMARY CONTAINER QUANTITY: 10

VERSED

MIDAZOLAM HYDROCHLORIDE INJECTION

NSN, MFG P/N

6505012801074

NSN

6505-01-280-1074

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VERSED

MIDAZOLAM HYDROCHLORIDE INJECTION

NSN, MFG P/N

6505012801074

NSN

6505-01-280-1074

MFG

HOFFMANN-LA ROCHE INC.

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 1.000 MILLIGRAM MIDAZOLAM EQUIVALENT PER MILLILITER
ADMINISTRATION: INTRAMUSCULAR OR INTRAVENOUS
FEATURES PROVIDED: STERILE
III CONTROLLED SUBSTANCE CLASSIFICATION: SCHEDULE IV
III PART NAME ASSIGNED BY CONTROLLING AGENCY: MIDAZOLAM HYDROCHLORIDE INJECTION 1MG EQUIV PER ML IV 2ML VIAL 10S
III PROTECTIVE STORAGE FEATURE: SECURITY STORAGE
PRIMARY CONTAINER CONTENT QUANTITY: 2.000 MILLILITERS
PRIMARY CONTAINER TYPE: VIAL
TOTAL PRIMARY CONTAINER QUANTITY: 10

013572

ASPIRIN,ALUMINUM HYDROXIDE GEL,DRIED,CALCIUM CARBONATE,AND MAGNESIUM HYDROXIDE TABLETS

NSN, MFG P/N

6505012801793

NSN

6505-01-280-1793

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013572

ASPIRIN,ALUMINUM HYDROXIDE GEL,DRIED,CALCIUM CARBONATE,AND MAGNESIUM HYDROXIDE TABLETS

NSN, MFG P/N

6505012801793

NSN

6505-01-280-1793

MFG

AVENTIS PHARMACEUTICALS PRODUCTS INC.

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 50.000 MILLIGRAMS ALUMINUM HYDROXIDE GEL, DRIED ACTIVE INGREDIENT AND 50.000 MILLIGRAMS MAGNESIUM HYDROXIDE ACTIVE INGREDIENT AND 87.000 MILLIGRAMS CALCIUM CARBONATE ACTIVE INGREDIENT AND 325.000 MILLIGRAMS ASPIRIN ACTIVE INGREDIENT
PRIMARY CONTAINER CONTENT QUANTITY: 2.000 TABLETS
SPECIAL FEATURES: PRIMARY CONTAINER TYPE:PACKET;
TOTAL PRIMARY CONTAINER QUANTITY: 250

ASCRIPTIN

ASPIRIN,ALUMINUM HYDROXIDE GEL,DRIED,CALCIUM CARBONATE,AND MAGNESIUM HYDROXIDE TABLETS

NSN, MFG P/N

6505012801793

NSN

6505-01-280-1793

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ASCRIPTIN

ASPIRIN,ALUMINUM HYDROXIDE GEL,DRIED,CALCIUM CARBONATE,AND MAGNESIUM HYDROXIDE TABLETS

NSN, MFG P/N

6505012801793

NSN

6505-01-280-1793

MFG

AVENTIS PHARMACEUTICALS PRODUCTS INC.

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 50.000 MILLIGRAMS ALUMINUM HYDROXIDE GEL, DRIED ACTIVE INGREDIENT AND 50.000 MILLIGRAMS MAGNESIUM HYDROXIDE ACTIVE INGREDIENT AND 87.000 MILLIGRAMS CALCIUM CARBONATE ACTIVE INGREDIENT AND 325.000 MILLIGRAMS ASPIRIN ACTIVE INGREDIENT
PRIMARY CONTAINER CONTENT QUANTITY: 2.000 TABLETS
SPECIAL FEATURES: PRIMARY CONTAINER TYPE:PACKET;
TOTAL PRIMARY CONTAINER QUANTITY: 250

NDC00067-0145-72

ASPIRIN,ALUMINUM HYDROXIDE GEL,DRIED,CALCIUM CARBONATE,AND MAGNESIUM HYDROXIDE TABLETS

NSN, MFG P/N

6505012801793

NSN

6505-01-280-1793

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NDC00067-0145-72

ASPIRIN,ALUMINUM HYDROXIDE GEL,DRIED,CALCIUM CARBONATE,AND MAGNESIUM HYDROXIDE TABLETS

NSN, MFG P/N

6505012801793

NSN

6505-01-280-1793

MFG

AVENTIS PHARMACEUTICALS PRODUCTS INC.

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 50.000 MILLIGRAMS ALUMINUM HYDROXIDE GEL, DRIED ACTIVE INGREDIENT AND 50.000 MILLIGRAMS MAGNESIUM HYDROXIDE ACTIVE INGREDIENT AND 87.000 MILLIGRAMS CALCIUM CARBONATE ACTIVE INGREDIENT AND 325.000 MILLIGRAMS ASPIRIN ACTIVE INGREDIENT
PRIMARY CONTAINER CONTENT QUANTITY: 2.000 TABLETS
SPECIAL FEATURES: PRIMARY CONTAINER TYPE:PACKET;
TOTAL PRIMARY CONTAINER QUANTITY: 250

NDC00378-0205-01

AMOXICILLIN CAPSULES,USP

NSN, MFG P/N

6505012802162

NSN

6505-01-280-2162

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NDC00378-0205-01

AMOXICILLIN CAPSULES,USP

NSN, MFG P/N

6505012802162

NSN

6505-01-280-2162

MFG

MYLAN PHARMACEUTICALS INC

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 500.000 MILLIGRAMS AMOXICILLIN ACTIVE INGREDIENT
ADMINISTRATION: ORAL
CAPSULE CONTENT FORM: ANY ACCEPTABLE
CAPSULE PRIMARY CONTAINER CONTENT QUANTITY: 100.000
CAPSULE TYPE: ANY ACCEPTABLE
PRIMARY CONTAINER TYPE: BOTTLE

NDC00206-3880-25

PIPERACILLIN SODIUM,USP

NSN, MFG P/N

6505012802318

NSN

6505-01-280-2318

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NDC00206-3880-25

PIPERACILLIN SODIUM,USP

NSN, MFG P/N

6505012802318

NSN

6505-01-280-2318

MFG

AMERICAN CYANAMID CO LEDERLE LABORATORIES DIV

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 4.000 GRAMS PIPERACILLIN EQUIVALENT
ADMINISTRATION: INTRAMUSCULAR OR INTRAVENOUS
III PART NAME ASSIGNED BY CONTROLLING AGENCY: PIPERACILLIN SODIUM STERILE USP 4GM POWDER INTRAMUSCLAR/IV VIAL 10S
PHYSICAL FORM: POWDER
PRIMARY CONTAINER CONTENT QUANTITY: 4.000 GRAMS OF ACTIVE INGREDIENT
PRIMARY CONTAINER TYPE: VIAL
TOTAL PRIMARY CONTAINER QUANTITY: 10