Product NDC: | 10888-5006 |
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, LIQUID FILLED |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 10888-5006 |
Labeler Name: | Banner Pharmacaps Inc |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA078720 |
Marketing Category: | ANDA |
Start Marketing Date: | 20121101 |
Package NDC: | 10888-5006-2 |
Package Description: | 100 CAPSULE, LIQUID FILLED in 1 BOTTLE (10888-5006-2) |
NDC Code | 10888-5006-2 |
Proprietary Name | Amantadine HCl |
Package Description | 100 CAPSULE, LIQUID FILLED in 1 BOTTLE (10888-5006-2) |
Product NDC | 10888-5006 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | AMANTADINE HYDROCHLORIDE |
Dosage Form Name | CAPSULE, LIQUID FILLED |
Route Name | ORAL |
Start Marketing Date | 20121101 |
Marketing Category Name | ANDA |
Labeler Name | Banner Pharmacaps Inc |
Substance Name | AMANTADINE HYDROCHLORIDE |
Strength Number | 100 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Influenza A M2 Protein Inhibitor [EPC],M2 Protein Inhibitors [MoA] |