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Atorvastatin Calcium
Atorvastatin Calcium - 51079-412-03 - (atorvastatin calcium)
Drug Information of Atorvastatin Calcium
| Product NDC: | 51079-412 |
| Proprietary Name: | Atorvastatin Calcium |
| Non Proprietary Name: | atorvastatin calcium |
| Active Ingredient(s): | 80 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: | 51079-412 |
| Labeler Name: | Mylan Institutional Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA091226 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20121227 |
Package Information of Atorvastatin Calcium
| Package NDC: | 51079-412-03 |
| Package Description: | 30 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-412-03) > 1 TABLET, FILM COATED in 1 BLISTER PACK (51079-412-01) |
NDC Information of Atorvastatin Calcium
| NDC Code | 51079-412-03 |
| Proprietary Name | Atorvastatin Calcium |
| Package Description | 30 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-412-03) > 1 TABLET, FILM COATED in 1 BLISTER PACK (51079-412-01) |
| Product NDC | 51079-412 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | atorvastatin calcium |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20121227 |
| Marketing Category Name | ANDA |
| Labeler Name | Mylan Institutional Inc. |
| Substance Name | ATORVASTATIN CALCIUM |
| Strength Number | 80 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | HMG-CoA Reductase Inhibitor [EPC],Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA] |
