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PRAVACHOL
PRAVACHOL - 0003-5194-10 - (PRAVASTATIN SODIUM)
Drug Information of PRAVACHOL
| Product NDC: | 0003-5194 |
| Proprietary Name: | PRAVACHOL |
| 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 PRAVACHOL
| Product NDC: | 0003-5194 |
| Labeler Name: | E.R. Squibb & Sons, L.L.C. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA019898 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20090601 |
Package Information of PRAVACHOL
| Package NDC: | 0003-5194-10 |
| Package Description: | 90 TABLET in 1 BOTTLE (0003-5194-10) |
NDC Information of PRAVACHOL
| NDC Code | 0003-5194-10 |
| Proprietary Name | PRAVACHOL |
| Package Description | 90 TABLET in 1 BOTTLE (0003-5194-10) |
| Product NDC | 0003-5194 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | PRAVASTATIN SODIUM |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20090601 |
| Marketing Category Name | NDA |
| Labeler Name | E.R. Squibb & Sons, L.L.C. |
| Substance Name | PRAVASTATIN SODIUM |
| Strength Number | 40 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | HMG-CoA Reductase Inhibitor [EPC],Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA] |
