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Simcor
Simcor - 0074-3312-07 - (Niacin and Simvastatin)
Drug Information of Simcor
| Product NDC: | 0074-3312 |
| Proprietary Name: | Simcor |
| Non Proprietary Name: | Niacin and Simvastatin |
| Active Ingredient(s): | 500; 20 mg/1; mg/1 & nbsp; Niacin and Simvastatin |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED, EXTENDED RELEASE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Simcor
| Product NDC: | 0074-3312 |
| Labeler Name: | AbbVie Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA022078 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20080215 |
Package Information of Simcor
| Package NDC: | 0074-3312-07 |
| Package Description: | 1 BOTTLE in 1 CARTON (0074-3312-07) > 7 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE |
NDC Information of Simcor
| NDC Code | 0074-3312-07 |
| Proprietary Name | Simcor |
| Package Description | 1 BOTTLE in 1 CARTON (0074-3312-07) > 7 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE |
| Product NDC | 0074-3312 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Niacin and Simvastatin |
| Dosage Form Name | TABLET, FILM COATED, EXTENDED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20080215 |
| Marketing Category Name | NDA |
| Labeler Name | AbbVie Inc. |
| Substance Name | NIACIN; SIMVASTATIN |
| Strength Number | 500; 20 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes | Nicotinic Acid [EPC],Nicotinic Acids [Chemical/Ingredient],HMG-CoA Reductase Inhibitor [EPC],Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA] |
