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6505-01-156-1600

20 Products

NDC00006-3239-66

CHLOROTHIAZIDE ORAL SUSPENSION,USP

NSN, MFG P/N

6505011561600

NSN

6505-01-156-1600

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NDC00006-3239-66

CHLOROTHIAZIDE ORAL SUSPENSION,USP

NSN, MFG P/N

6505011561600

NSN

6505-01-156-1600

MFG

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

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 250.000 MILLIGRAMS CHLOROTHIAZIDE PER 5 MILLILITERS
III PART NAME ASSIGNED BY CONTROLLING AGENCY: CHLOROTHIAZIDE ORAL SUSPENSION USP 250MG/5ML 237ML BT
III PROTECTIVE STORAGE FEATURE: SUBJECT TO DAMAGE BY FREEZING
PRIMARY CONTAINER CONTENT QUANTITY: 237.000 MILLILITERS
PRIMARY CONTAINER TYPE: BOTTLE

0859

CEFOPERAZONE SODIUM,USP

NSN, MFG P/N

6505011559431

NSN

6505-01-155-9431

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0859

CEFOPERAZONE SODIUM,USP

NSN, MFG P/N

6505011559431

NSN

6505-01-155-9431

MFG

ROERIG DIV PFIZER INC

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 2 GM. CEFOPERAZONE EQUIV. OF BASE IN VIAL
ADMINISTRATION: INTRAMUSCULAR OR INTRAVENOUS
III PART NAME ASSIGNED BY CONTROLLING AGENCY: CEFOPERAZONE SODIUM STERILE USP POWDER FORM 2GM VIAL 10S
PHYSICAL FORM: POWDER
PRIMARY CONTAINER CONTENT QUANTITY: POWDER SUFFICIENT TO YIELD 2 GM. CEFOPERAZONE
PRIMARY CONTAINER TYPE: VIAL
TOTAL SECONDARY CONTAINER QUANTITY: 10

CEFOBID

CEFOPERAZONE SODIUM,USP

NSN, MFG P/N

6505011559431

NSN

6505-01-155-9431

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CEFOBID

CEFOPERAZONE SODIUM,USP

NSN, MFG P/N

6505011559431

NSN

6505-01-155-9431

MFG

ROERIG DIV PFIZER INC

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 2 GM. CEFOPERAZONE EQUIV. OF BASE IN VIAL
ADMINISTRATION: INTRAMUSCULAR OR INTRAVENOUS
III PART NAME ASSIGNED BY CONTROLLING AGENCY: CEFOPERAZONE SODIUM STERILE USP POWDER FORM 2GM VIAL 10S
PHYSICAL FORM: POWDER
PRIMARY CONTAINER CONTENT QUANTITY: POWDER SUFFICIENT TO YIELD 2 GM. CEFOPERAZONE
PRIMARY CONTAINER TYPE: VIAL
TOTAL SECONDARY CONTAINER QUANTITY: 10

NDC00049-1202-83

CEFOPERAZONE SODIUM,USP

NSN, MFG P/N

6505011559431

NSN

6505-01-155-9431

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NDC00049-1202-83

CEFOPERAZONE SODIUM,USP

NSN, MFG P/N

6505011559431

NSN

6505-01-155-9431

MFG

ROERIG DIV PFIZER INC

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 2 GM. CEFOPERAZONE EQUIV. OF BASE IN VIAL
ADMINISTRATION: INTRAMUSCULAR OR INTRAVENOUS
III PART NAME ASSIGNED BY CONTROLLING AGENCY: CEFOPERAZONE SODIUM STERILE USP POWDER FORM 2GM VIAL 10S
PHYSICAL FORM: POWDER
PRIMARY CONTAINER CONTENT QUANTITY: POWDER SUFFICIENT TO YIELD 2 GM. CEFOPERAZONE
PRIMARY CONTAINER TYPE: VIAL
TOTAL SECONDARY CONTAINER QUANTITY: 10

LITHONATE CAPSULES

LITHIUM CARBONATE CAPSULES,USP

NSN, MFG P/N

6505011559434

NSN

6505-01-155-9434

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LITHONATE CAPSULES

LITHIUM CARBONATE CAPSULES,USP

NSN, MFG P/N

6505011559434

NSN

6505-01-155-9434

MFG

SOLVAY PHARMACEUTICALS INC.

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 300.000 MILLIGRAMS LITHIUM CARBONATE ACTIVE INGREDIENT
CAPSULE CONTENT FORM: ANY ACCEPTABLE
CAPSULE PRIMARY CONTAINER CONTENT QUANTITY: 120.000
CAPSULE TYPE: ANY ACCEPTABLE
FEATURES PROVIDED: TAMPER PROOF
PRIMARY CONTAINER TYPE: BOTTLE
SPECIAL FEATURES: WITH 3-PART LABEL

NDC00032-7512-12

LITHIUM CARBONATE CAPSULES,USP

NSN, MFG P/N

6505011559434

NSN

6505-01-155-9434

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NDC00032-7512-12

LITHIUM CARBONATE CAPSULES,USP

NSN, MFG P/N

6505011559434

NSN

6505-01-155-9434

MFG

SOLVAY PHARMACEUTICALS INC.

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 300.000 MILLIGRAMS LITHIUM CARBONATE ACTIVE INGREDIENT
CAPSULE CONTENT FORM: ANY ACCEPTABLE
CAPSULE PRIMARY CONTAINER CONTENT QUANTITY: 120.000
CAPSULE TYPE: ANY ACCEPTABLE
FEATURES PROVIDED: TAMPER PROOF
PRIMARY CONTAINER TYPE: BOTTLE
SPECIAL FEATURES: WITH 3-PART LABEL

LITHONATE CAPSULES

LITHIUM CARBONATE CAPSULES,USP

NSN, MFG P/N

6505011559435

NSN

6505-01-155-9435

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LITHONATE CAPSULES

LITHIUM CARBONATE CAPSULES,USP

NSN, MFG P/N

6505011559435

NSN

6505-01-155-9435

MFG

SOLVAY PHARMACEUTICALS INC.

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 300.000 MILLIGRAMS LITHIUM CARBONATE ACTIVE INGREDIENT
CAPSULE CONTENT FORM: ANY ACCEPTABLE
CAPSULE PRIMARY CONTAINER CONTENT QUANTITY: 90.000
CAPSULE TYPE: ANY ACCEPTABLE
FEATURES PROVIDED: TAMPER PROOF
PRIMARY CONTAINER TYPE: BOTTLE
SPECIAL FEATURES: WITH 3-PART LABEL

NDC00032-7512-09

LITHIUM CARBONATE CAPSULES,USP

NSN, MFG P/N

6505011559435

NSN

6505-01-155-9435

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NDC00032-7512-09

LITHIUM CARBONATE CAPSULES,USP

NSN, MFG P/N

6505011559435

NSN

6505-01-155-9435

MFG

SOLVAY PHARMACEUTICALS INC.

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 300.000 MILLIGRAMS LITHIUM CARBONATE ACTIVE INGREDIENT
CAPSULE CONTENT FORM: ANY ACCEPTABLE
CAPSULE PRIMARY CONTAINER CONTENT QUANTITY: 90.000
CAPSULE TYPE: ANY ACCEPTABLE
FEATURES PROVIDED: TAMPER PROOF
PRIMARY CONTAINER TYPE: BOTTLE
SPECIAL FEATURES: WITH 3-PART LABEL

6505-00-C99-7553

DEXTROSE,POTASSIUM CHLORIDE,AND SODIUM CHLORIDE INJECTION

NSN, MFG P/N

6505011559436

NSN

6505-01-155-9436

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6505-00-C99-7553

DEXTROSE,POTASSIUM CHLORIDE,AND SODIUM CHLORIDE INJECTION

NSN, MFG P/N

6505011559436

NSN

6505-01-155-9436

MFG

DEFENSE LOGISTICS AGENCY DIRECTORATE OF MEDICAL MATERIEL DEFENSE SUPPLY CENTER PHILADELPHIA

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 5.000 PERCENTAGE, W/V DEXTROSE ACTIVE INGREDIENT AND 0.300 PERCENTAGE, W/V POTASSIUM CHLORIDE ACTIVE INGREDIENT AND 0.225 PERCENTAGE, W/V SODIUM CHLORIDE ACTIVE INGREDIENT
PRIMARY CONTAINER CONTENT QUANTITY: 1000.000 MILLILITERS
PRIMARY CONTAINER TYPE: BOTTLE, GLASS
TOTAL PRIMARY CONTAINER QUANTITY: 6

NDC00074-5846-05

DEXTROSE,POTASSIUM CHLORIDE,AND SODIUM CHLORIDE INJECTION

NSN, MFG P/N

6505011559436

NSN

6505-01-155-9436

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NDC00074-5846-05

DEXTROSE,POTASSIUM CHLORIDE,AND SODIUM CHLORIDE INJECTION

NSN, MFG P/N

6505011559436

NSN

6505-01-155-9436

MFG

ABBOTT LABORATORIES INC. DIV HOSPITAL PRODUCTS DIVISION

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 5.000 PERCENTAGE, W/V DEXTROSE ACTIVE INGREDIENT AND 0.300 PERCENTAGE, W/V POTASSIUM CHLORIDE ACTIVE INGREDIENT AND 0.225 PERCENTAGE, W/V SODIUM CHLORIDE ACTIVE INGREDIENT
PRIMARY CONTAINER CONTENT QUANTITY: 1000.000 MILLILITERS
PRIMARY CONTAINER TYPE: BOTTLE, GLASS
TOTAL PRIMARY CONTAINER QUANTITY: 6

NDC50111-0621-01

KETOCONAZOLE TABLETS,USP

NSN, MFG P/N

6505011560701

NSN

6505-01-156-0701

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NDC50111-0621-01

KETOCONAZOLE TABLETS,USP

NSN, MFG P/N

6505011560701

NSN

6505-01-156-0701

MFG

PLIVA INC .

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 200.000 MILLIGRAMS KETOCONAZOLE ACTIVE INGREDIENT
III PART NAME ASSIGNED BY CONTROLLING AGENCY: KETOCONAZOLE TABLETS USP 200MG 100S BT
PRIMARY CONTAINER CONTENT QUANTITY: 100.000 TABLETS
PRIMARY CONTAINER TYPE: BOTTLE
SUPPLEMENTARY FEATURES: D-DAY ITEM FOR DOD

NDC51672-4026-01

KETOCONAZOLE TABLETS,USP

NSN, MFG P/N

6505011560701

NSN

6505-01-156-0701

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NDC51672-4026-01

KETOCONAZOLE TABLETS,USP

NSN, MFG P/N

6505011560701

NSN

6505-01-156-0701

MFG

TARO PHARMACEUTICALS INC

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 200.000 MILLIGRAMS KETOCONAZOLE ACTIVE INGREDIENT
III PART NAME ASSIGNED BY CONTROLLING AGENCY: KETOCONAZOLE TABLETS USP 200MG 100S BT
PRIMARY CONTAINER CONTENT QUANTITY: 100.000 TABLETS
PRIMARY CONTAINER TYPE: BOTTLE
SUPPLEMENTARY FEATURES: D-DAY ITEM FOR DOD

NDC60505-0092-00

KETOCONAZOLE TABLETS,USP

NSN, MFG P/N

6505011560701

NSN

6505-01-156-0701

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NDC60505-0092-00

KETOCONAZOLE TABLETS,USP

NSN, MFG P/N

6505011560701

NSN

6505-01-156-0701

MFG

APOTEX INC

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 200.000 MILLIGRAMS KETOCONAZOLE ACTIVE INGREDIENT
III PART NAME ASSIGNED BY CONTROLLING AGENCY: KETOCONAZOLE TABLETS USP 200MG 100S BT
PRIMARY CONTAINER CONTENT QUANTITY: 100.000 TABLETS
PRIMARY CONTAINER TYPE: BOTTLE
SUPPLEMENTARY FEATURES: D-DAY ITEM FOR DOD

15A

OPIUM,POWDERED AND BELLADONNA EXTRACT SUPPOSITORIES

NSN, MFG P/N

6505011561588

NSN

6505-01-156-1588

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15A

OPIUM,POWDERED AND BELLADONNA EXTRACT SUPPOSITORIES

NSN, MFG P/N

6505011561588

NSN

6505-01-156-1588

MFG

POLYMEDICA CORPORATION

Description

ACTIVE INGREDIENT AND STRENGTH: 30.000 OPIUM, POWDERED MILLIGRAMS AND 16.200 BELLADONNA EXTRACT, POWDERED MILLIGRAMS
III PART NAME ASSIGNED BY CONTROLLING AGENCY: OPIUM POWDERED & BELLADONNA EXTRACT SUPPOSITORIES ADULT RECTAL 12S
PRIMARY CONTAINER TYPE: STRIP
SUPPOSITORY TYPE: ADULT RECTAL
UNIT PACKAGE QUANTITY: 12 SUPPOSITORIES PER PACKAGE

B AND O SUPPRETTES

OPIUM,POWDERED AND BELLADONNA EXTRACT SUPPOSITORIES

NSN, MFG P/N

6505011561588

NSN

6505-01-156-1588

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B AND O SUPPRETTES

OPIUM,POWDERED AND BELLADONNA EXTRACT SUPPOSITORIES

NSN, MFG P/N

6505011561588

NSN

6505-01-156-1588

MFG

POLYMEDICA CORPORATION

Description

ACTIVE INGREDIENT AND STRENGTH: 30.000 OPIUM, POWDERED MILLIGRAMS AND 16.200 BELLADONNA EXTRACT, POWDERED MILLIGRAMS
III PART NAME ASSIGNED BY CONTROLLING AGENCY: OPIUM POWDERED & BELLADONNA EXTRACT SUPPOSITORIES ADULT RECTAL 12S
PRIMARY CONTAINER TYPE: STRIP
SUPPOSITORY TYPE: ADULT RECTAL
UNIT PACKAGE QUANTITY: 12 SUPPOSITORIES PER PACKAGE

NDC00574-7045-12

OPIUM,POWDERED AND BELLADONNA EXTRACT SUPPOSITORIES

NSN, MFG P/N

6505011561588

NSN

6505-01-156-1588

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NDC00574-7045-12

OPIUM,POWDERED AND BELLADONNA EXTRACT SUPPOSITORIES

NSN, MFG P/N

6505011561588

NSN

6505-01-156-1588

MFG

PADDOCK LABORATORIES INC.

Description

ACTIVE INGREDIENT AND STRENGTH: 30.000 OPIUM, POWDERED MILLIGRAMS AND 16.200 BELLADONNA EXTRACT, POWDERED MILLIGRAMS
III PART NAME ASSIGNED BY CONTROLLING AGENCY: OPIUM POWDERED & BELLADONNA EXTRACT SUPPOSITORIES ADULT RECTAL 12S
PRIMARY CONTAINER TYPE: STRIP
SUPPOSITORY TYPE: ADULT RECTAL
UNIT PACKAGE QUANTITY: 12 SUPPOSITORIES PER PACKAGE

NDC61451-5015-07

OPIUM,POWDERED AND BELLADONNA EXTRACT SUPPOSITORIES

NSN, MFG P/N

6505011561588

NSN

6505-01-156-1588

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NDC61451-5015-07

OPIUM,POWDERED AND BELLADONNA EXTRACT SUPPOSITORIES

NSN, MFG P/N

6505011561588

NSN

6505-01-156-1588

MFG

POLYMEDICA CORPORATION

Description

ACTIVE INGREDIENT AND STRENGTH: 30.000 OPIUM, POWDERED MILLIGRAMS AND 16.200 BELLADONNA EXTRACT, POWDERED MILLIGRAMS
III PART NAME ASSIGNED BY CONTROLLING AGENCY: OPIUM POWDERED & BELLADONNA EXTRACT SUPPOSITORIES ADULT RECTAL 12S
PRIMARY CONTAINER TYPE: STRIP
SUPPOSITORY TYPE: ADULT RECTAL
UNIT PACKAGE QUANTITY: 12 SUPPOSITORIES PER PACKAGE

MAXIDEX

DEXAMETHASONE OPHTHALMIC SUSPENSION,USP

NSN, MFG P/N

6505011561595

NSN

6505-01-156-1595

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MAXIDEX

DEXAMETHASONE OPHTHALMIC SUSPENSION,USP

NSN, MFG P/N

6505011561595

NSN

6505-01-156-1595

MFG

ALCON LABORATORIES INC .

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 0.100 PERCENTAGE, W/V DEXAMETHASONE ACTIVE INGREDIENT
FEATURES PROVIDED: STERILE
PRIMARY CONTAINER CONTENT QUANTITY: 15.000 MILLILITERS
PRIMARY CONTAINER TYPE: BOTTLE WITH OPHTHALMIC TIP
SPECIAL FEATURES: MEDSEP ITEM FOR DOD,ALCON LABS INC

NDC00998-0615-15

DEXAMETHASONE OPHTHALMIC SUSPENSION,USP

NSN, MFG P/N

6505011561595

NSN

6505-01-156-1595

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NDC00998-0615-15

DEXAMETHASONE OPHTHALMIC SUSPENSION,USP

NSN, MFG P/N

6505011561595

NSN

6505-01-156-1595

MFG

ALCON LABORATORIES INC .

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 0.100 PERCENTAGE, W/V DEXAMETHASONE ACTIVE INGREDIENT
FEATURES PROVIDED: STERILE
PRIMARY CONTAINER CONTENT QUANTITY: 15.000 MILLILITERS
PRIMARY CONTAINER TYPE: BOTTLE WITH OPHTHALMIC TIP
SPECIAL FEATURES: MEDSEP ITEM FOR DOD,ALCON LABS INC

DIURIL

CHLOROTHIAZIDE ORAL SUSPENSION,USP

NSN, MFG P/N

6505011561600

NSN

6505-01-156-1600

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DIURIL

CHLOROTHIAZIDE ORAL SUSPENSION,USP

NSN, MFG P/N

6505011561600

NSN

6505-01-156-1600

MFG

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

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 250.000 MILLIGRAMS CHLOROTHIAZIDE PER 5 MILLILITERS
III PART NAME ASSIGNED BY CONTROLLING AGENCY: CHLOROTHIAZIDE ORAL SUSPENSION USP 250MG/5ML 237ML BT
III PROTECTIVE STORAGE FEATURE: SUBJECT TO DAMAGE BY FREEZING
PRIMARY CONTAINER CONTENT QUANTITY: 237.000 MILLILITERS
PRIMARY CONTAINER TYPE: BOTTLE