Product NDC: | 49999-306 |
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) |
Product NDC: | 49999-306 |
Labeler Name: | Lake Erie Medical Surgical & Supply DBA Quality Care Products LLC |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA019766 |
Marketing Category: | NDA |
Start Marketing Date: | 20110808 |
Package NDC: | 49999-306-30 |
Package Description: | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (49999-306-30) |
NDC Code | 49999-306-30 |
Proprietary Name | ZOCOR |
Package Description | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (49999-306-30) |
Product NDC | 49999-306 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | simvastatin |
Dosage Form Name | TABLET, FILM COATED |
Route Name | ORAL |
Start Marketing Date | 20110808 |
Marketing Category Name | NDA |
Labeler Name | Lake Erie Medical Surgical & Supply DBA Quality Care Products LLC |
Substance Name | SIMVASTATIN |
Strength Number | 20 |
Strength Unit | mg/1 |
Pharmaceutical Classes | HMG-CoA Reductase Inhibitor [EPC],Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA] |