# Pravastatin Sodium

NDC: 69292-103
Generic name: Pravastatin Sodium
Labeler / Manufacturer: Amici Pharma, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20260519

FDA application: ANDA077491

## Active ingredients

- PRAVASTATIN SODIUM: 40 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"69292-103"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=69292-103
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=e6551230-fe4c-4a6e-9c19-ae9945b76db0