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Sodium Chloride - 63323-186-02 - (SODIUM CHLORIDE)

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Drug Information of Sodium Chloride

Product NDC: 63323-186
Proprietary Name: 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 Sodium Chloride

Product NDC: 63323-186
Labeler Name: APP Pharmaceuticals, LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date: 20000810

Package Information of Sodium Chloride

Package NDC: 63323-186-02
Package Description: 25 VIAL, SINGLE-DOSE in 1 TRAY (63323-186-02) > 2 mL in 1 VIAL, SINGLE-DOSE

NDC Information of Sodium Chloride

NDC Code 63323-186-02
Proprietary Name Sodium Chloride
Package Description 25 VIAL, SINGLE-DOSE in 1 TRAY (63323-186-02) > 2 mL in 1 VIAL, SINGLE-DOSE
Product NDC 63323-186
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name SODIUM CHLORIDE
Dosage Form Name INJECTION
Route Name INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS
Start Marketing Date 20000810
Marketing Category Name UNAPPROVED DRUG OTHER
Labeler Name APP Pharmaceuticals, LLC
Substance Name SODIUM CHLORIDE
Strength Number 9
Strength Unit mg/mL
Pharmaceutical Classes

Complete Information of Sodium Chloride


General Information