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ZOCOR
ZOCOR - 0006-0740-54 - (SIMVASTATIN)
Drug Information of ZOCOR
| Product NDC: | 0006-0740 |
| Proprietary Name: | ZOCOR |
| Non Proprietary Name: | SIMVASTATIN |
| Active Ingredient(s): | 20 mg/1 & nbsp; SIMVASTATIN |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of ZOCOR
| Product NDC: | 0006-0740 |
| Labeler Name: | Merck Sharp & Dohme Corp. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA019766 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19911223 |
Package Information of ZOCOR
| Package NDC: | 0006-0740-54 |
| Package Description: | 90 TABLET, FILM COATED in 1 BOTTLE (0006-0740-54) |
NDC Information of ZOCOR
| NDC Code | 0006-0740-54 |
| Proprietary Name | ZOCOR |
| Package Description | 90 TABLET, FILM COATED in 1 BOTTLE (0006-0740-54) |
| Product NDC | 0006-0740 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | SIMVASTATIN |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 19911223 |
| Marketing Category Name | NDA |
| Labeler Name | Merck Sharp & Dohme Corp. |
| Substance Name | SIMVASTATIN |
| Strength Number | 20 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | HMG-CoA Reductase Inhibitor [EPC],Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA] |
