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SULAR
SULAR - 59630-501-10 - (Nisoldipine)
Drug Information of SULAR
| Product NDC: | 59630-501 |
| Proprietary Name: | SULAR |
| 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 SULAR
| Product NDC: | 59630-501 |
| Labeler Name: | Shionogi Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020356 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19950202 |
Package Information of SULAR
| Package NDC: | 59630-501-10 |
| Package Description: | 1 BOTTLE in 1 CARTON (59630-501-10) > 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE |
NDC Information of SULAR
| NDC Code | 59630-501-10 |
| Proprietary Name | SULAR |
| Package Description | 1 BOTTLE in 1 CARTON (59630-501-10) > 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE |
| Product NDC | 59630-501 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Nisoldipine |
| Dosage Form Name | TABLET, FILM COATED, EXTENDED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 19950202 |
| Marketing Category Name | NDA |
| Labeler Name | Shionogi 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] |
