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Nisoldipine
Nisoldipine - 0378-2223-05 - (Nisoldipine)
Drug Information of Nisoldipine
| Product NDC: | 0378-2223 |
| Proprietary Name: | Nisoldipine |
| Non Proprietary Name: | Nisoldipine |
| Active Ingredient(s): | 30 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: | 0378-2223 |
| Labeler Name: | Mylan Pharmaceuticals Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA079051 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20120829 |
Package Information of Nisoldipine
| Package NDC: | 0378-2223-05 |
| Package Description: | 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0378-2223-05) |
NDC Information of Nisoldipine
| NDC Code | 0378-2223-05 |
| Proprietary Name | Nisoldipine |
| Package Description | 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0378-2223-05) |
| Product NDC | 0378-2223 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Nisoldipine |
| Dosage Form Name | TABLET, FILM COATED, EXTENDED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20120829 |
| Marketing Category Name | ANDA |
| Labeler Name | Mylan Pharmaceuticals Inc. |
| Substance Name | NISOLDIPINE |
| Strength Number | 30 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Dihydropyridine Calcium Channel Blocker [EPC],Dihydropyridines [Chemical/Ingredient],Calcium Channel Antagonists [MoA],Decreased Blood Pressure [PE] |
