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Bacteriostatic Sodium Chloride - 63323-924-10 - (SODIUM CHLORIDE)

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Drug Information of Bacteriostatic Sodium Chloride

Product NDC: 63323-924
Proprietary Name: Bacteriostatic Sodium Chloride
Non Proprietary Name: SODIUM CHLORIDE
Active Ingredient(s): 9    mg/mL & nbsp;   SODIUM CHLORIDE
Administration Route(s): INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS
Dosage Form(s): INJECTION
Coding System: National Drug Codes(NDC)

Labeler Information of Bacteriostatic Sodium Chloride

Product NDC: 63323-924
Labeler Name: APP Pharmaceuticals, LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA088911
Marketing Category: ANDA
Start Marketing Date: 20000808

Package Information of Bacteriostatic Sodium Chloride

Package NDC: 63323-924-10
Package Description: 25 VIAL, MULTI-DOSE in 1 TRAY (63323-924-10) > 10 mL in 1 VIAL, MULTI-DOSE

NDC Information of Bacteriostatic Sodium Chloride

NDC Code 63323-924-10
Proprietary Name Bacteriostatic Sodium Chloride
Package Description 25 VIAL, MULTI-DOSE in 1 TRAY (63323-924-10) > 10 mL in 1 VIAL, MULTI-DOSE
Product NDC 63323-924
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name SODIUM CHLORIDE
Dosage Form Name INJECTION
Route Name INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS
Start Marketing Date 20000808
Marketing Category Name ANDA
Labeler Name APP Pharmaceuticals, LLC
Substance Name SODIUM CHLORIDE
Strength Number 9
Strength Unit mg/mL
Pharmaceutical Classes

Complete Information of Bacteriostatic Sodium Chloride


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