Home > National Drug Code (NDC) > Amantadine HCl

Amantadine HCl - 21695-564-10 - (Amantadine hydrochloride)

Alphabetical Index


Drug Information of Amantadine HCl

Product NDC: 21695-564
Proprietary Name: Amantadine HCl
Non Proprietary Name: Amantadine hydrochloride
Active Ingredient(s): 100    mg/1 & nbsp;   Amantadine hydrochloride
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Amantadine HCl

Product NDC: 21695-564
Labeler Name: Rebel Distributors Corp.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078720
Marketing Category: ANDA
Start Marketing Date: 20081101

Package Information of Amantadine HCl

Package NDC: 21695-564-10
Package Description: 10 CAPSULE in 1 BOTTLE (21695-564-10)

NDC Information of Amantadine HCl

NDC Code 21695-564-10
Proprietary Name Amantadine HCl
Package Description 10 CAPSULE in 1 BOTTLE (21695-564-10)
Product NDC 21695-564
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Amantadine hydrochloride
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20081101
Marketing Category Name ANDA
Labeler Name Rebel Distributors Corp.
Substance Name AMANTADINE HYDROCHLORIDE
Strength Number 100
Strength Unit mg/1
Pharmaceutical Classes Influenza A M2 Protein Inhibitor [EPC],M2 Protein Inhibitors [MoA]

Complete Information of Amantadine HCl


General Information