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PRAVASTATIN SODIUM
PRAVASTATIN SODIUM - 60505-0170-8 - (PRAVASTATIN SODIUM)
Drug Information of PRAVASTATIN SODIUM
| Product NDC: | 60505-0170 |
| Proprietary Name: | PRAVASTATIN SODIUM |
| Non Proprietary Name: | PRAVASTATIN SODIUM |
| Active Ingredient(s): | 40 mg/1 & nbsp; PRAVASTATIN SODIUM |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of PRAVASTATIN SODIUM
| Product NDC: | 60505-0170 |
| Labeler Name: | Apotex Corp. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA076341 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20110718 |
Package Information of PRAVASTATIN SODIUM
| Package NDC: | 60505-0170-8 |
| Package Description: | 9000 TABLET in 1 BOTTLE (60505-0170-8) |
NDC Information of PRAVASTATIN SODIUM
| NDC Code | 60505-0170-8 |
| Proprietary Name | PRAVASTATIN SODIUM |
| Package Description | 9000 TABLET in 1 BOTTLE (60505-0170-8) |
| Product NDC | 60505-0170 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | PRAVASTATIN SODIUM |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20110718 |
| Marketing Category Name | ANDA |
| Labeler Name | Apotex Corp. |
| Substance Name | PRAVASTATIN SODIUM |
| Strength Number | 40 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | HMG-CoA Reductase Inhibitor [EPC],Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA] |
