Home
>
National Drug Code (NDC)
>
Amantadine Hydrochloride
Amantadine Hydrochloride - 50383-807-16 - (Amantadine Hydrochloride)
Drug Information of Amantadine Hydrochloride
| Product NDC: | 50383-807 |
| Proprietary Name: | Amantadine Hydrochloride |
| Non Proprietary Name: | Amantadine Hydrochloride |
| Active Ingredient(s): | 50 mg/5mL & nbsp; Amantadine Hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Amantadine Hydrochloride
| Product NDC: | 50383-807 |
| Labeler Name: | Hi-Tech Pharmacal Co., Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA074170 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19941028 |
Package Information of Amantadine Hydrochloride
| Package NDC: | 50383-807-16 |
| Package Description: | 473 mL in 1 BOTTLE (50383-807-16) |
NDC Information of Amantadine Hydrochloride
| NDC Code | 50383-807-16 |
| Proprietary Name | Amantadine Hydrochloride |
| Package Description | 473 mL in 1 BOTTLE (50383-807-16) |
| Product NDC | 50383-807 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Amantadine Hydrochloride |
| Dosage Form Name | SOLUTION |
| Route Name | ORAL |
| Start Marketing Date | 19941028 |
| Marketing Category Name | ANDA |
| Labeler Name | Hi-Tech Pharmacal Co., Inc. |
| Substance Name | AMANTADINE HYDROCHLORIDE |
| Strength Number | 50 |
| Strength Unit | mg/5mL |
| Pharmaceutical Classes | Influenza A M2 Protein Inhibitor [EPC],M2 Protein Inhibitors [MoA] |
