Home
>
National Drug Code (NDC)
>
Pravastatin sodium
Pravastatin sodium - 55111-229-01 - (Pravastatin sodium)
Drug Information of Pravastatin sodium
| Product NDC: | 55111-229 |
| 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: | 55111-229 |
| 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: | 55111-229-01 |
| Package Description: | 100 TABLET in 1 BOTTLE (55111-229-01) |
NDC Information of Pravastatin sodium
| NDC Code | 55111-229-01 |
| Proprietary Name | Pravastatin sodium |
| Package Description | 100 TABLET in 1 BOTTLE (55111-229-01) |
| Product NDC | 55111-229 |
| 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 | 10 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | HMG-CoA Reductase Inhibitor [EPC],Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA] |
