Details for New Drug Application (NDA): 077730
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The generic ingredient in PRAVASTATIN SODIUM is pravastatin sodium. There are sixteen drug master file entries for this compound. Forty-one suppliers are listed for this compound. Additional details are available on the pravastatin sodium profile page.
Summary for 077730
Tradename: | PRAVASTATIN SODIUM |
Applicant: | Pliva Hrvatska Doo |
Ingredient: | pravastatin sodium |
Patents: | 0 |
Medical Subject Heading (MeSH) Categories for 077730
Profile for product number 001
Active Rx/OTC/Discontinued: | DISCN | Dosage: | TABLET;ORAL | Strength | 10MG | ||||
Approval Date: | Nov 21, 2006 | TE: | RLD: | No |
Profile for product number 002
Active Rx/OTC/Discontinued: | DISCN | Dosage: | TABLET;ORAL | Strength | 20MG | ||||
Approval Date: | Nov 21, 2006 | TE: | RLD: | No |
Profile for product number 003
Active Rx/OTC/Discontinued: | DISCN | Dosage: | TABLET;ORAL | Strength | 30MG | ||||
Approval Date: | Nov 21, 2006 | TE: | RLD: | No |
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