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ATORVASTATIN CALCIUM
ATORVASTATIN CALCIUM - 0591-3775-51 - (ATORVASTATIN CALCIUM)
Drug Information of ATORVASTATIN CALCIUM
| Product NDC: | 0591-3775 |
| Proprietary Name: | ATORVASTATIN CALCIUM |
| Non Proprietary Name: | ATORVASTATIN CALCIUM |
| Active Ingredient(s): | 20 mg/1 & nbsp; ATORVASTATIN CALCIUM |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of ATORVASTATIN CALCIUM
| Product NDC: | 0591-3775 |
| Labeler Name: | Watson Laboratories, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020702 |
| Marketing Category: | NDA AUTHORIZED GENERIC |
| Start Marketing Date: | 20111130 |
Package Information of ATORVASTATIN CALCIUM
| Package NDC: | 0591-3775-51 |
| Package Description: | 5000 TABLET, FILM COATED in 1 BOTTLE (0591-3775-51) |
NDC Information of ATORVASTATIN CALCIUM
| NDC Code | 0591-3775-51 |
| Proprietary Name | ATORVASTATIN CALCIUM |
| Package Description | 5000 TABLET, FILM COATED in 1 BOTTLE (0591-3775-51) |
| Product NDC | 0591-3775 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | ATORVASTATIN CALCIUM |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20111130 |
| Marketing Category Name | NDA AUTHORIZED GENERIC |
| Labeler Name | Watson Laboratories, Inc. |
| Substance Name | ATORVASTATIN CALCIUM |
| Strength Number | 20 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | HMG-CoA Reductase Inhibitor [EPC],Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA] |
