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Sodium Chloride Hypertonicity - 0904-5314-35 - (sodium chloride)

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Drug Information of Sodium Chloride Hypertonicity

Product NDC: 0904-5314
Proprietary Name: Sodium Chloride Hypertonicity
Non Proprietary Name: sodium chloride
Active Ingredient(s): 50    mg/mL & nbsp;   sodium chloride
Administration Route(s): OPHTHALMIC
Dosage Form(s): SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Sodium Chloride Hypertonicity

Product NDC: 0904-5314
Labeler Name: Major Pharmaceuticals
Product Type: HUMAN OTC DRUG
FDA Application Number: part349
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20110101

Package Information of Sodium Chloride Hypertonicity

Package NDC: 0904-5314-35
Package Description: 1 BOTTLE in 1 CARTON (0904-5314-35) > 15 mL in 1 BOTTLE

NDC Information of Sodium Chloride Hypertonicity

NDC Code 0904-5314-35
Proprietary Name Sodium Chloride Hypertonicity
Package Description 1 BOTTLE in 1 CARTON (0904-5314-35) > 15 mL in 1 BOTTLE
Product NDC 0904-5314
Product Type Name HUMAN OTC DRUG
Non Proprietary Name sodium chloride
Dosage Form Name SOLUTION
Route Name OPHTHALMIC
Start Marketing Date 20110101
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Major Pharmaceuticals
Substance Name SODIUM CHLORIDE
Strength Number 50
Strength Unit mg/mL
Pharmaceutical Classes

Complete Information of Sodium Chloride Hypertonicity


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