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Sodium Chloride - 0487-9301-03 - (ISodium Chloride)

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Drug Information of Sodium Chloride

Product NDC: 0487-9301
Proprietary Name: Sodium Chloride
Non Proprietary Name: ISodium Chloride
Active Ingredient(s): .027    mg/3mL & nbsp;   ISodium Chloride
Administration Route(s): RESPIRATORY (INHALATION)
Dosage Form(s): SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Sodium Chloride

Product NDC: 0487-9301
Labeler Name: Nephron Pharmaceuticals Corporation
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date: 20020718

Package Information of Sodium Chloride

Package NDC: 0487-9301-03
Package Description: 100 VIAL, SINGLE-USE in 1 CARTON (0487-9301-03) > 3 mL in 1 VIAL, SINGLE-USE

NDC Information of Sodium Chloride

NDC Code 0487-9301-03
Proprietary Name Sodium Chloride
Package Description 100 VIAL, SINGLE-USE in 1 CARTON (0487-9301-03) > 3 mL in 1 VIAL, SINGLE-USE
Product NDC 0487-9301
Product Type Name HUMAN OTC DRUG
Non Proprietary Name ISodium Chloride
Dosage Form Name SOLUTION
Route Name RESPIRATORY (INHALATION)
Start Marketing Date 20020718
Marketing Category Name UNAPPROVED DRUG OTHER
Labeler Name Nephron Pharmaceuticals Corporation
Substance Name SODIUM CHLORIDE
Strength Number .027
Strength Unit mg/3mL
Pharmaceutical Classes

Complete Information of Sodium Chloride


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