| 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] |