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Sodium Chloride - 0264-7802-00 - (SODIUM CHLORIDE)

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Drug Information of Sodium Chloride

Product NDC: 0264-7802
Proprietary Name: Sodium Chloride
Non Proprietary Name: SODIUM CHLORIDE
Active Ingredient(s): .45    g/100mL & nbsp;   SODIUM CHLORIDE
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Sodium Chloride

Product NDC: 0264-7802
Labeler Name: B. Braun Medical Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA019635
Marketing Category: NDA
Start Marketing Date: 19880309

Package Information of Sodium Chloride

Package NDC: 0264-7802-00
Package Description: 12 CONTAINER in 1 CASE (0264-7802-00) > 1000 mL in 1 CONTAINER

NDC Information of Sodium Chloride

NDC Code 0264-7802-00
Proprietary Name Sodium Chloride
Package Description 12 CONTAINER in 1 CASE (0264-7802-00) > 1000 mL in 1 CONTAINER
Product NDC 0264-7802
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name SODIUM CHLORIDE
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 19880309
Marketing Category Name NDA
Labeler Name B. Braun Medical Inc.
Substance Name SODIUM CHLORIDE
Strength Number .45
Strength Unit g/100mL
Pharmaceutical Classes

Complete Information of Sodium Chloride


General Information