Home
>
National Drug Code (NDC)
>
Rimantadine Hydrochloride
Rimantadine Hydrochloride - 52959-305-30 - (Rimantadine Hydrochloride)
Drug Information of Rimantadine Hydrochloride
| Product NDC: | 52959-305 |
| Proprietary Name: | Rimantadine Hydrochloride |
| Non Proprietary Name: | Rimantadine Hydrochloride |
| Active Ingredient(s): | 100 mg/1 & nbsp; Rimantadine Hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Rimantadine Hydrochloride
| Product NDC: | 52959-305 |
| Labeler Name: | H.J. Harkins Company, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA076132 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20050401 |
Package Information of Rimantadine Hydrochloride
| Package NDC: | 52959-305-30 |
| Package Description: | 30 TABLET, FILM COATED in 1 BOTTLE (52959-305-30) |
NDC Information of Rimantadine Hydrochloride
| NDC Code | 52959-305-30 |
| Proprietary Name | Rimantadine Hydrochloride |
| Package Description | 30 TABLET, FILM COATED in 1 BOTTLE (52959-305-30) |
| Product NDC | 52959-305 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Rimantadine Hydrochloride |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20050401 |
| Marketing Category Name | ANDA |
| Labeler Name | H.J. Harkins Company, Inc. |
| Substance Name | RIMANTADINE HYDROCHLORIDE |
| Strength Number | 100 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Influenza A M2 Protein Inhibitor [EPC],M2 Protein Inhibitors [MoA] |
