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Rimantadine Hydrochloride - 0115-1911-02 - (Rimantadine Hydrochloride)

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Drug Information of Rimantadine Hydrochloride

Product NDC: 0115-1911
Proprietary Name: Rimantadine Hydrochloride
Non Proprietary Name: Rimantadine Hydrochloride
Active Ingredient(s): 100    mg/1 & nbsp;   Rimantadine Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Rimantadine Hydrochloride

Product NDC: 0115-1911
Labeler Name: Global Pharmaceuticals, Division of Impax Laboratories Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076132
Marketing Category: ANDA
Start Marketing Date: 20050401

Package Information of Rimantadine Hydrochloride

Package NDC: 0115-1911-02
Package Description: 500 TABLET, FILM COATED in 1 BOTTLE (0115-1911-02)

NDC Information of Rimantadine Hydrochloride

NDC Code 0115-1911-02
Proprietary Name Rimantadine Hydrochloride
Package Description 500 TABLET, FILM COATED in 1 BOTTLE (0115-1911-02)
Product NDC 0115-1911
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Rimantadine Hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20050401
Marketing Category Name ANDA
Labeler Name Global Pharmaceuticals, Division of Impax Laboratories Inc.
Substance Name RIMANTADINE HYDROCHLORIDE
Strength Number 100
Strength Unit mg/1
Pharmaceutical Classes Influenza A M2 Protein Inhibitor [EPC],M2 Protein Inhibitors [MoA]

Complete Information of Rimantadine Hydrochloride


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