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6505-01-097-4766

20 Products

NDC17314-9330-01

SODIUM CITRATE AND CITRIC ACID ORAL SOLUTION,USP

NSN, MFG P/N

6505010974766

NSN

6505-01-097-4766

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NDC17314-9330-01

SODIUM CITRATE AND CITRIC ACID ORAL SOLUTION,USP

NSN, MFG P/N

6505010974766

NSN

6505-01-097-4766

MFG

CARDINAL HEALTH INC. DBA CARDINAL HEALTH

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 1500.000 MG SODIUM CITRATE,DIHYDRATE PER 15 ML AND 1002.000 MG CITRIC ACID,MONOHYDRATE PER 15 ML
III PART NAME ASSIGNED BY CONTROLLING AGENCY: SODIUM CITRATE AND CITRIC ACID ORAL SOLUTION USP 473ML BT
PRIMARY CONTAINER CONTENT QUANTITY: 16.000 FLUID OUNCES OR 473.000 MILLILITERS
PRIMARY CONTAINER TYPE: BOTTLE
SPECIAL FEATURES: EACH ML CONTAINS 1 MEQ SODIUM ION AND IS EQUIVALENT TO 1 MEQ BICARBONATE (HCO3)

NEBULO 28

WATER FOR INHALATION,STERILE,USP

NSN, MFG P/N

6505010970001

NSN

6505-01-097-0001

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NEBULO 28

WATER FOR INHALATION,STERILE,USP

NSN, MFG P/N

6505010970001

NSN

6505-01-097-0001

MFG

BARD C R INC INSPIRON DIV

Description

III PART NAME ASSIGNED BY CONTROLLING AGENCY: WATER FOR INHALATION STERILE USP 1000ML BT 12 PER PG
III SUPPLEMENTARY FEATURES: MEDSEP ITEM FOR DOD,BAXTER HEALTHCARE
PRIMARY CONTAINER CONTENT QUANTITY: 1000.000 MILLILITERS
PRIMARY CONTAINER TYPE: BOTTLE, PLASTIC
SPECIAL FEATURES: WITH NEBULIZER ADAPTER
TOTAL PRIMARY CONTAINER QUANTITY: 12

NDC00641-0422-25

HYDROXYZINE HYDROCHLORIDE INJECTION,USP

NSN, MFG P/N

6505010970002

NSN

6505-01-097-0002

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NDC00641-0422-25

HYDROXYZINE HYDROCHLORIDE INJECTION,USP

NSN, MFG P/N

6505010970002

NSN

6505-01-097-0002

MFG

ELKINS-SINN INC

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 50.000 MILLIGRAMS HYDROXYZINE HYDROCHLORIDE PER MILLILITER
ADMINISTRATION: INTRAMUSCULAR
FEATURES PROVIDED: STERILE
III PART NAME ASSIGNED BY CONTROLLING AGENCY: HYDROXYZINE HYDROCHLORIDE INJECTION USP 50MG/ML 1ML BT 25 PER PG
III SUPPLEMENTARY FEATURES: MEDSEP ITEM FOR DOOD,ELKINS-SINN
PRIMARY CONTAINER CONTENT QUANTITY: 1.000 MILLILITERS
PRIMARY CONTAINER TYPE: BOTTLE
TOTAL PRIMARY CONTAINER QUANTITY: 25

NDC00641-0433-25

HYDROXYZINE HYDROCHLORIDE INJECTION,USP

NSN, MFG P/N

6505010970002

NSN

6505-01-097-0002

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NDC00641-0433-25

HYDROXYZINE HYDROCHLORIDE INJECTION,USP

NSN, MFG P/N

6505010970002

NSN

6505-01-097-0002

MFG

ELKINS-SINN INC

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 50.000 MILLIGRAMS HYDROXYZINE HYDROCHLORIDE PER MILLILITER
ADMINISTRATION: INTRAMUSCULAR
FEATURES PROVIDED: STERILE
III PART NAME ASSIGNED BY CONTROLLING AGENCY: HYDROXYZINE HYDROCHLORIDE INJECTION USP 50MG/ML 1ML BT 25 PER PG
III SUPPLEMENTARY FEATURES: MEDSEP ITEM FOR DOOD,ELKINS-SINN
PRIMARY CONTAINER CONTENT QUANTITY: 1.000 MILLILITERS
PRIMARY CONTAINER TYPE: BOTTLE
TOTAL PRIMARY CONTAINER QUANTITY: 25

019-0954-T3

IOTHALAMATE SODIUM INJECTION,USP

NSN, MFG P/N

6505010970668

NSN

6505-01-097-0668

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019-0954-T3

IOTHALAMATE SODIUM INJECTION,USP

NSN, MFG P/N

6505010970668

NSN

6505-01-097-0668

MFG

MALLINCKRODT INC ANESTHESIA PRODUCTS

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 66.800 PERCENTAGE, W/V IOTHALAMATE SODIUM ACTIVE INGREDIENT
III EXTERIOR CONTAINER CUBIC MEASURE: 0.767 CUBIC FEET
III EXTERIOR CONTAINER QUANTITY: 1
III EXTERIOR CONTAINER WEIGHT: 18.00 POUNDS
III PART NAME ASSIGNED BY CONTROLLING AGENCY: IOTHALAMATE SODIUM INJECTION USP 66.8% 50ML VIAL 50 PER PG
III PROTECTIVE STORAGE FEATURE: SUBJECT TO DAMAGE BY FREEZING
III SUPPLEMENTARY FEATURES: RADIOPAQUE CONTRAST MEDIUM FOR INTRAVENOUS UROGRAPHY INTRAVASCULAR ANGIOCARDIOGRAPHY AND AORTOGRAPHY
III UNIT OF ISSUE CUBE: 0.005 CUBIC FEET
III UNIT OF ISSUE WEIGHT: 0.06 POUNDS
PHARMACEUTICAL VEHICLE TYPE: AQUEOUS
PRIMARY CONTAINER CONTENT QUANTITY: 50.000 MILLILITERS
PRIMARY CONTAINER TYPE: VIAL
TOTAL PRIMARY CONTAINER QUANTITY: 50
UNIT PACKAGE TYPE: PACKAGE

CONRAY-400

IOTHALAMATE SODIUM INJECTION,USP

NSN, MFG P/N

6505010970668

NSN

6505-01-097-0668

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CONRAY-400

IOTHALAMATE SODIUM INJECTION,USP

NSN, MFG P/N

6505010970668

NSN

6505-01-097-0668

MFG

MALLINCKRODT INC ANESTHESIA PRODUCTS

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 66.800 PERCENTAGE, W/V IOTHALAMATE SODIUM ACTIVE INGREDIENT
III EXTERIOR CONTAINER CUBIC MEASURE: 0.767 CUBIC FEET
III EXTERIOR CONTAINER QUANTITY: 1
III EXTERIOR CONTAINER WEIGHT: 18.00 POUNDS
III PART NAME ASSIGNED BY CONTROLLING AGENCY: IOTHALAMATE SODIUM INJECTION USP 66.8% 50ML VIAL 50 PER PG
III PROTECTIVE STORAGE FEATURE: SUBJECT TO DAMAGE BY FREEZING
III SUPPLEMENTARY FEATURES: RADIOPAQUE CONTRAST MEDIUM FOR INTRAVENOUS UROGRAPHY INTRAVASCULAR ANGIOCARDIOGRAPHY AND AORTOGRAPHY
III UNIT OF ISSUE CUBE: 0.005 CUBIC FEET
III UNIT OF ISSUE WEIGHT: 0.06 POUNDS
PHARMACEUTICAL VEHICLE TYPE: AQUEOUS
PRIMARY CONTAINER CONTENT QUANTITY: 50.000 MILLILITERS
PRIMARY CONTAINER TYPE: VIAL
TOTAL PRIMARY CONTAINER QUANTITY: 50
UNIT PACKAGE TYPE: PACKAGE

NDC00019-0954-15

IOTHALAMATE SODIUM INJECTION,USP

NSN, MFG P/N

6505010970668

NSN

6505-01-097-0668

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NDC00019-0954-15

IOTHALAMATE SODIUM INJECTION,USP

NSN, MFG P/N

6505010970668

NSN

6505-01-097-0668

MFG

MALLINCKRODT INC ANESTHESIA PRODUCTS

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 66.800 PERCENTAGE, W/V IOTHALAMATE SODIUM ACTIVE INGREDIENT
III EXTERIOR CONTAINER CUBIC MEASURE: 0.767 CUBIC FEET
III EXTERIOR CONTAINER QUANTITY: 1
III EXTERIOR CONTAINER WEIGHT: 18.00 POUNDS
III PART NAME ASSIGNED BY CONTROLLING AGENCY: IOTHALAMATE SODIUM INJECTION USP 66.8% 50ML VIAL 50 PER PG
III PROTECTIVE STORAGE FEATURE: SUBJECT TO DAMAGE BY FREEZING
III SUPPLEMENTARY FEATURES: RADIOPAQUE CONTRAST MEDIUM FOR INTRAVENOUS UROGRAPHY INTRAVASCULAR ANGIOCARDIOGRAPHY AND AORTOGRAPHY
III UNIT OF ISSUE CUBE: 0.005 CUBIC FEET
III UNIT OF ISSUE WEIGHT: 0.06 POUNDS
PHARMACEUTICAL VEHICLE TYPE: AQUEOUS
PRIMARY CONTAINER CONTENT QUANTITY: 50.000 MILLILITERS
PRIMARY CONTAINER TYPE: VIAL
TOTAL PRIMARY CONTAINER QUANTITY: 50
UNIT PACKAGE TYPE: PACKAGE

CUPRIMINE

PENICILLAMINE CAPSULES,USP

NSN, MFG P/N

6505010971232

NSN

6505-01-097-1232

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CUPRIMINE

PENICILLAMINE CAPSULES,USP

NSN, MFG P/N

6505010971232

NSN

6505-01-097-1232

MFG

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

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 125.000 MILLIGRAMS PENICILLAMINE ACTIVE INGREDIENT
CAPSULE CONTENT FORM: ANY ACCEPTABLE
CAPSULE PRIMARY CONTAINER CONTENT QUANTITY: 100.000
CAPSULE TYPE: ANY ACCEPTABLE
III PART NAME ASSIGNED BY CONTROLLING AGENCY: PENICILLAMINE CAPSULES USP 125MG 100S BT
PRIMARY CONTAINER TYPE: BOTTLE

CUPRIMINE CAPSULES

PENICILLAMINE CAPSULES,USP

NSN, MFG P/N

6505010971232

NSN

6505-01-097-1232

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CUPRIMINE CAPSULES

PENICILLAMINE CAPSULES,USP

NSN, MFG P/N

6505010971232

NSN

6505-01-097-1232

MFG

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

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 125.000 MILLIGRAMS PENICILLAMINE ACTIVE INGREDIENT
CAPSULE CONTENT FORM: ANY ACCEPTABLE
CAPSULE PRIMARY CONTAINER CONTENT QUANTITY: 100.000
CAPSULE TYPE: ANY ACCEPTABLE
III PART NAME ASSIGNED BY CONTROLLING AGENCY: PENICILLAMINE CAPSULES USP 125MG 100S BT
PRIMARY CONTAINER TYPE: BOTTLE

NDC00006-0672-68

PENICILLAMINE CAPSULES,USP

NSN, MFG P/N

6505010971232

NSN

6505-01-097-1232

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NDC00006-0672-68

PENICILLAMINE CAPSULES,USP

NSN, MFG P/N

6505010971232

NSN

6505-01-097-1232

MFG

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

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 125.000 MILLIGRAMS PENICILLAMINE ACTIVE INGREDIENT
CAPSULE CONTENT FORM: ANY ACCEPTABLE
CAPSULE PRIMARY CONTAINER CONTENT QUANTITY: 100.000
CAPSULE TYPE: ANY ACCEPTABLE
III PART NAME ASSIGNED BY CONTROLLING AGENCY: PENICILLAMINE CAPSULES USP 125MG 100S BT
PRIMARY CONTAINER TYPE: BOTTLE

NDC00006-0650-68

CARBIDOPA AND LEVODOPA TABLETS,USP

NSN, MFG P/N

6505010971233

NSN

6505-01-097-1233

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NDC00006-0650-68

CARBIDOPA AND LEVODOPA TABLETS,USP

NSN, MFG P/N

6505010971233

NSN

6505-01-097-1233

MFG

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

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 25.000 MILLIGRAMS CARBIDOPA ACTIVE INGREDIENT AND 100.000 MILLIGRAMS LEVODOPA ACTIVE INGREDIENT
ADMINISTRATION: ORAL
III PART NAME ASSIGNED BY CONTROLLING AGENCY: CARBIDOPA AND LEVODOPA TABLETS USP 100S BT
PRIMARY CONTAINER CONTENT QUANTITY: 100.000 TABLETS
PRIMARY CONTAINER TYPE: BOTTLE

NDC00056-0650-68

CARBIDOPA AND LEVODOPA TABLETS,USP

NSN, MFG P/N

6505010971233

NSN

6505-01-097-1233

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NDC00056-0650-68

CARBIDOPA AND LEVODOPA TABLETS,USP

NSN, MFG P/N

6505010971233

NSN

6505-01-097-1233

MFG

BRISTOL-MYERS SQUIBB PHARMA COMPANY

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 25.000 MILLIGRAMS CARBIDOPA ACTIVE INGREDIENT AND 100.000 MILLIGRAMS LEVODOPA ACTIVE INGREDIENT
ADMINISTRATION: ORAL
III PART NAME ASSIGNED BY CONTROLLING AGENCY: CARBIDOPA AND LEVODOPA TABLETS USP 100S BT
PRIMARY CONTAINER CONTENT QUANTITY: 100.000 TABLETS
PRIMARY CONTAINER TYPE: BOTTLE

SINEMET

CARBIDOPA AND LEVODOPA TABLETS,USP

NSN, MFG P/N

6505010971233

NSN

6505-01-097-1233

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SINEMET

CARBIDOPA AND LEVODOPA TABLETS,USP

NSN, MFG P/N

6505010971233

NSN

6505-01-097-1233

MFG

BRISTOL-MYERS SQUIBB PHARMA COMPANY

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 25.000 MILLIGRAMS CARBIDOPA ACTIVE INGREDIENT AND 100.000 MILLIGRAMS LEVODOPA ACTIVE INGREDIENT
ADMINISTRATION: ORAL
III PART NAME ASSIGNED BY CONTROLLING AGENCY: CARBIDOPA AND LEVODOPA TABLETS USP 100S BT
PRIMARY CONTAINER CONTENT QUANTITY: 100.000 TABLETS
PRIMARY CONTAINER TYPE: BOTTLE

SINEMET TABLETS

CARBIDOPA AND LEVODOPA TABLETS,USP

NSN, MFG P/N

6505010971233

NSN

6505-01-097-1233

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SINEMET TABLETS

CARBIDOPA AND LEVODOPA TABLETS,USP

NSN, MFG P/N

6505010971233

NSN

6505-01-097-1233

MFG

BRISTOL-MYERS SQUIBB PHARMA COMPANY

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 25.000 MILLIGRAMS CARBIDOPA ACTIVE INGREDIENT AND 100.000 MILLIGRAMS LEVODOPA ACTIVE INGREDIENT
ADMINISTRATION: ORAL
III PART NAME ASSIGNED BY CONTROLLING AGENCY: CARBIDOPA AND LEVODOPA TABLETS USP 100S BT
PRIMARY CONTAINER CONTENT QUANTITY: 100.000 TABLETS
PRIMARY CONTAINER TYPE: BOTTLE

NDC11538-2019-00

IODINE COMPLEX SOLUTION

NSN, MFG P/N

6505010971335

NSN

6505-01-097-1335

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NDC11538-2019-00

IODINE COMPLEX SOLUTION

NSN, MFG P/N

6505010971335

NSN

6505-01-097-1335

MFG

AMERICAN STERILIZER COMPANY DBA AMSCO STERILITY ASSURANCE PRODUCTS

Description

(NON-CORE DATA) UNIT PACKAGE TYPE: BOTTLE, PLASTIC
QUANTITY WITHIN EACH UNIT PACKAGE: 6.0 FLUID OUNCES
SOLUTE EQUIVALENT IN PERCENT: 1.0 IODINE
UNIT PACKAGE QUANTITY: 1 BOTTLE

NH004

IODINE COMPLEX SOLUTION

NSN, MFG P/N

6505010971335

NSN

6505-01-097-1335

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NH004

IODINE COMPLEX SOLUTION

NSN, MFG P/N

6505010971335

NSN

6505-01-097-1335

MFG

AMERICAN STERILIZER COMPANY DBA AMSCO STERILITY ASSURANCE PRODUCTS

Description

(NON-CORE DATA) UNIT PACKAGE TYPE: BOTTLE, PLASTIC
QUANTITY WITHIN EACH UNIT PACKAGE: 6.0 FLUID OUNCES
SOLUTE EQUIVALENT IN PERCENT: 1.0 IODINE
UNIT PACKAGE QUANTITY: 1 BOTTLE

PREPODYNE SOLUTION

IODINE COMPLEX SOLUTION

NSN, MFG P/N

6505010971335

NSN

6505-01-097-1335

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PREPODYNE SOLUTION

IODINE COMPLEX SOLUTION

NSN, MFG P/N

6505010971335

NSN

6505-01-097-1335

MFG

AMERICAN STERILIZER COMPANY DBA AMSCO STERILITY ASSURANCE PRODUCTS

Description

(NON-CORE DATA) UNIT PACKAGE TYPE: BOTTLE, PLASTIC
QUANTITY WITHIN EACH UNIT PACKAGE: 6.0 FLUID OUNCES
SOLUTE EQUIVALENT IN PERCENT: 1.0 IODINE
UNIT PACKAGE QUANTITY: 1 BOTTLE

NDC00015-3072-20

CISPLATIN FOR INJECTION

NSN, MFG P/N

6505010972935

NSN

6505-01-097-2935

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NDC00015-3072-20

CISPLATIN FOR INJECTION

NSN, MFG P/N

6505010972935

NSN

6505-01-097-2935

MFG

MEAD JOHNSON & COMPANY DBA MEAD JOHNSON NUTRITIONALS

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 50.000 MILLIGRAMS CISPLATIN ACTIVE INGREDIENT
III PROTECTIVE STORAGE FEATURE: ANTINEOPLASTIC DRUG
PHYSICAL FORM: POWDER
PRIMARY CONTAINER CONTENT QUANTITY: 50.000 MILLIGRAMS
PRIMARY CONTAINER TYPE: VIAL

PLATINOL

CISPLATIN FOR INJECTION

NSN, MFG P/N

6505010972935

NSN

6505-01-097-2935

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PLATINOL

CISPLATIN FOR INJECTION

NSN, MFG P/N

6505010972935

NSN

6505-01-097-2935

MFG

MEAD JOHNSON & COMPANY DBA MEAD JOHNSON NUTRITIONALS

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 50.000 MILLIGRAMS CISPLATIN ACTIVE INGREDIENT
III PROTECTIVE STORAGE FEATURE: ANTINEOPLASTIC DRUG
PHYSICAL FORM: POWDER
PRIMARY CONTAINER CONTENT QUANTITY: 50.000 MILLIGRAMS
PRIMARY CONTAINER TYPE: VIAL

NDC00121-0595-16

SODIUM CITRATE AND CITRIC ACID ORAL SOLUTION,USP

NSN, MFG P/N

6505010974766

NSN

6505-01-097-4766

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NDC00121-0595-16

SODIUM CITRATE AND CITRIC ACID ORAL SOLUTION,USP

NSN, MFG P/N

6505010974766

NSN

6505-01-097-4766

MFG

PHARMACEUTICAL ASSOCIATES INC

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 1500.000 MG SODIUM CITRATE,DIHYDRATE PER 15 ML AND 1002.000 MG CITRIC ACID,MONOHYDRATE PER 15 ML
III PART NAME ASSIGNED BY CONTROLLING AGENCY: SODIUM CITRATE AND CITRIC ACID ORAL SOLUTION USP 473ML BT
PRIMARY CONTAINER CONTENT QUANTITY: 16.000 FLUID OUNCES OR 473.000 MILLILITERS
PRIMARY CONTAINER TYPE: BOTTLE
SPECIAL FEATURES: EACH ML CONTAINS 1 MEQ SODIUM ION AND IS EQUIVALENT TO 1 MEQ BICARBONATE (HCO3)