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simvastatin
simvastatin - 49349-925-38 - (simvastatin)
Drug Information of simvastatin
| Product NDC: | 49349-925 |
| Proprietary Name: | simvastatin |
| 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 simvastatin
| Product NDC: | 49349-925 |
| Labeler Name: | REMEDYREPACK INC. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA078155 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20130514 |
Package Information of simvastatin
| Package NDC: | 49349-925-38 |
| Package Description: | 3 TABLET, FILM COATED in 1 BLISTER PACK (49349-925-38) |
NDC Information of simvastatin
| NDC Code | 49349-925-38 |
| Proprietary Name | simvastatin |
| Package Description | 3 TABLET, FILM COATED in 1 BLISTER PACK (49349-925-38) |
| Product NDC | 49349-925 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | simvastatin |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20130514 |
| Marketing Category Name | ANDA |
| Labeler Name | REMEDYREPACK INC. |
| Substance Name | SIMVASTATIN |
| Strength Number | 20 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | HMG-CoA Reductase Inhibitor [EPC],Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA] |
