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PRAVASTATIN SODIUM
PRAVASTATIN SODIUM - 68180-485-02 - (PRAVASTATIN SODIUM)
Drug Information of PRAVASTATIN SODIUM
| Product NDC: | 68180-485 |
| Proprietary Name: | PRAVASTATIN SODIUM |
| Non Proprietary Name: | PRAVASTATIN SODIUM |
| Active Ingredient(s): | 10 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: | 68180-485 |
| Labeler Name: | Lupin Pharmaceuticals, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA077917 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20080724 |
Package Information of PRAVASTATIN SODIUM
| Package NDC: | 68180-485-02 |
| Package Description: | 500 TABLET in 1 BOTTLE (68180-485-02) |
NDC Information of PRAVASTATIN SODIUM
| NDC Code | 68180-485-02 |
| Proprietary Name | PRAVASTATIN SODIUM |
| Package Description | 500 TABLET in 1 BOTTLE (68180-485-02) |
| Product NDC | 68180-485 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | PRAVASTATIN SODIUM |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20080724 |
| Marketing Category Name | ANDA |
| Labeler Name | Lupin Pharmaceuticals, Inc. |
| Substance Name | PRAVASTATIN SODIUM |
| Strength Number | 10 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | HMG-CoA Reductase Inhibitor [EPC],Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA] |
