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Sodium Chloride - 55154-3183-8 - (Sodium Chloride)

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Drug Information of Sodium Chloride

Product NDC: 55154-3183
Proprietary Name: Sodium Chloride
Non Proprietary Name: Sodium Chloride
Active Ingredient(s): 9    mg/mL & nbsp;   Sodium Chloride
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION
Coding System: National Drug Codes(NDC)

Labeler Information of Sodium Chloride

Product NDC: 55154-3183
Labeler Name: Cardinal Health
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA018800
Marketing Category: NDA
Start Marketing Date: 19821029

Package Information of Sodium Chloride

Package NDC: 55154-3183-8
Package Description: 1 VIAL, MULTI-DOSE in 1 BAG (55154-3183-8) > 30 mL in 1 VIAL, MULTI-DOSE

NDC Information of Sodium Chloride

NDC Code 55154-3183-8
Proprietary Name Sodium Chloride
Package Description 1 VIAL, MULTI-DOSE in 1 BAG (55154-3183-8) > 30 mL in 1 VIAL, MULTI-DOSE
Product NDC 55154-3183
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Sodium Chloride
Dosage Form Name INJECTION
Route Name INTRAVENOUS
Start Marketing Date 19821029
Marketing Category Name NDA
Labeler Name Cardinal Health
Substance Name SODIUM CHLORIDE
Strength Number 9
Strength Unit mg/mL
Pharmaceutical Classes

Complete Information of Sodium Chloride


General Information