# Pravastatin Sodium

NDC: 0093-7201
Generic name: Pravastatin Sodium
Labeler / Manufacturer: Teva Pharmaceuticals USA, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20060425
Marketing ended: 20261231
FDA application: ANDA076056

## Active ingredients

- PRAVASTATIN SODIUM: 20 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0093-7201"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0093-7201
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=99e0e848-f8f3-4b42-b880-8fbc42633948