NDC 53808-0766
Pravastatin Sodium 20 mg tablet
On the label: State of Florida DOH Central Pharmacy. It's repackaged: State of Florida DOH Central Pharmacy rebottles it from Teva Pharmaceuticals USA, Inc.'s NDC 0093-7201.
Where the pills inside were made
This label doesn't name the factory that makes the drug. Companies don't have to print it on the label. The maker's name is often on the stock bottle your pharmacy used; you can ask the pharmacist. See the plants Teva Pharmaceuticals USA, Inc. names for other drugs.
Product details
- Generic drug
- Pravastatin: every company that makes it
- Form
- tablet
- Strength
- 20 mg
- Approval
- ANDA ANDA076056
- On the market since
- Jul 1, 2009
- Package NDCs
53808-0766-1- Official label
- DailyMed (National Library of Medicine), updated Jun 1, 2010
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