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Bacteriostatic Water - 49349-739-01 - (WATER)

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Drug Information of Bacteriostatic Water

Product NDC: 49349-739
Proprietary Name: Bacteriostatic Water
Non Proprietary Name: WATER
Active Ingredient(s): 1    mL/mL & nbsp;   WATER
Administration Route(s): INTRAMUSCULAR
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Bacteriostatic Water

Product NDC: 49349-739
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA018802
Marketing Category: NDA
Start Marketing Date: 20130610

Package Information of Bacteriostatic Water

Package NDC: 49349-739-01
Package Description: 30 mL in 1 VIAL (49349-739-01)

NDC Information of Bacteriostatic Water

NDC Code 49349-739-01
Proprietary Name Bacteriostatic Water
Package Description 30 mL in 1 VIAL (49349-739-01)
Product NDC 49349-739
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name WATER
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAMUSCULAR
Start Marketing Date 20130610
Marketing Category Name NDA
Labeler Name REMEDYREPACK INC.
Substance Name WATER
Strength Number 1
Strength Unit mL/mL
Pharmaceutical Classes

Complete Information of Bacteriostatic Water


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