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Amantadine Hydrochloride - 0603-1011-58 - (Amantadine Hydrochloride)

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Drug Information of Amantadine Hydrochloride

Product NDC: 0603-1011
Proprietary Name: Amantadine Hydrochloride
Non Proprietary Name: Amantadine Hydrochloride
Active Ingredient(s): 50    mg/5mL & nbsp;   Amantadine Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Amantadine Hydrochloride

Product NDC: 0603-1011
Labeler Name: Qualitest Pharmaceuticals
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077992
Marketing Category: ANDA
Start Marketing Date: 20061212

Package Information of Amantadine Hydrochloride

Package NDC: 0603-1011-58
Package Description: 473 mL in 1 BOTTLE (0603-1011-58)

NDC Information of Amantadine Hydrochloride

NDC Code 0603-1011-58
Proprietary Name Amantadine Hydrochloride
Package Description 473 mL in 1 BOTTLE (0603-1011-58)
Product NDC 0603-1011
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Amantadine Hydrochloride
Dosage Form Name SOLUTION
Route Name ORAL
Start Marketing Date 20061212
Marketing Category Name ANDA
Labeler Name Qualitest Pharmaceuticals
Substance Name AMANTADINE HYDROCHLORIDE
Strength Number 50
Strength Unit mg/5mL
Pharmaceutical Classes Influenza A M2 Protein Inhibitor [EPC],M2 Protein Inhibitors [MoA]

Complete Information of Amantadine Hydrochloride


General Information