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ATORVASTATIN CALCIUM
ATORVASTATIN CALCIUM - 68084-589-01 - (ATORVASTATIN CALCIUM)
Drug Information of ATORVASTATIN CALCIUM
| Product NDC: | 68084-589 |
| Proprietary Name: | ATORVASTATIN CALCIUM |
| Non Proprietary Name: | ATORVASTATIN CALCIUM |
| Active Ingredient(s): | 40 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: | 68084-589 |
| Labeler Name: | American Health Packaging |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020702 |
| Marketing Category: | NDA AUTHORIZED GENERIC |
| Start Marketing Date: | 20130705 |
Package Information of ATORVASTATIN CALCIUM
| Package NDC: | 68084-589-01 |
| Package Description: | 10 BLISTER PACK in 1 CARTON (68084-589-01) > 10 TABLET, FILM COATED in 1 BLISTER PACK (68084-589-11) |
NDC Information of ATORVASTATIN CALCIUM
| NDC Code | 68084-589-01 |
| Proprietary Name | ATORVASTATIN CALCIUM |
| Package Description | 10 BLISTER PACK in 1 CARTON (68084-589-01) > 10 TABLET, FILM COATED in 1 BLISTER PACK (68084-589-11) |
| Product NDC | 68084-589 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | ATORVASTATIN CALCIUM |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20130705 |
| Marketing Category Name | NDA AUTHORIZED GENERIC |
| Labeler Name | American Health Packaging |
| Substance Name | ATORVASTATIN CALCIUM |
| Strength Number | 40 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | HMG-CoA Reductase Inhibitor [EPC],Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA] |
