Home
>
National Drug Code (NDC)
>
Nisoldipine
Nisoldipine - 0677-1979-01 - (Nisoldipine)
Drug Information of Nisoldipine
| Product NDC: | 0677-1979 |
| Proprietary Name: | Nisoldipine |
| Non Proprietary Name: | Nisoldipine |
| Active Ingredient(s): | 17 mg/1 & nbsp; Nisoldipine |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED, EXTENDED RELEASE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Nisoldipine
| Product NDC: | 0677-1979 |
| Labeler Name: | United Research Laboratories, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020356 |
| Marketing Category: | NDA AUTHORIZED GENERIC |
| Start Marketing Date: | 20090901 |
Package Information of Nisoldipine
| Package NDC: | 0677-1979-01 |
| Package Description: | 1 BOTTLE in 1 CARTON (0677-1979-01) > 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE |
NDC Information of Nisoldipine
| NDC Code | 0677-1979-01 |
| Proprietary Name | Nisoldipine |
| Package Description | 1 BOTTLE in 1 CARTON (0677-1979-01) > 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE |
| Product NDC | 0677-1979 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Nisoldipine |
| Dosage Form Name | TABLET, FILM COATED, EXTENDED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20090901 |
| Marketing Category Name | NDA AUTHORIZED GENERIC |
| Labeler Name | United Research Laboratories, Inc. |
| Substance Name | NISOLDIPINE |
| Strength Number | 17 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Dihydropyridine Calcium Channel Blocker [EPC],Dihydropyridines [Chemical/Ingredient],Calcium Channel Antagonists [MoA],Decreased Blood Pressure [PE] |
