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Pravastatin sodium
Pravastatin sodium - 55111-231-30 - (Pravastatin sodium)
Drug Information of Pravastatin sodium
| Product NDC: | 55111-231 |
| 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: | 55111-231 |
| Labeler Name: | Dr.Reddy's Laboratories Limited |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA076714 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20091231 |
Package Information of Pravastatin sodium
| Package NDC: | 55111-231-30 |
| Package Description: | 30 TABLET in 1 BOTTLE (55111-231-30) |
NDC Information of Pravastatin sodium
| NDC Code | 55111-231-30 |
| Proprietary Name | Pravastatin sodium |
| Package Description | 30 TABLET in 1 BOTTLE (55111-231-30) |
| Product NDC | 55111-231 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Pravastatin sodium |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20091231 |
| Marketing Category Name | ANDA |
| Labeler Name | Dr.Reddy's Laboratories Limited |
| Substance Name | PRAVASTATIN SODIUM |
| Strength Number | 40 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | HMG-CoA Reductase Inhibitor [EPC],Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA] |
