| Product NDC: | 16590-008 |
| Proprietary Name: | AMANTADINE HYDROCHLORIDE |
| 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) |
| Product NDC: | 16590-008 |
| Labeler Name: | STAT RX USA LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA071293 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19870218 |
| Package NDC: | 16590-008-10 |
| Package Description: | 10 CAPSULE in 1 BOTTLE (16590-008-10) |
| NDC Code | 16590-008-10 |
| Proprietary Name | AMANTADINE HYDROCHLORIDE |
| Package Description | 10 CAPSULE in 1 BOTTLE (16590-008-10) |
| Product NDC | 16590-008 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | AMANTADINE HYDROCHLORIDE |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 19870218 |
| Marketing Category Name | ANDA |
| Labeler Name | STAT RX USA LLC |
| Substance Name | AMANTADINE HYDROCHLORIDE |
| Strength Number | 100 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Influenza A M2 Protein Inhibitor [EPC],M2 Protein Inhibitors [MoA] |