# Pravastatin Sodium

NDC: 60687-190
Generic name: Pravastatin Sodium
Labeler / Manufacturer: American Health Packaging
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20170215
Marketing ended: 20260630
FDA application: ANDA077987

## 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:"60687-190"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=60687-190
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=056475c8-59c2-469c-9175-7162065726f5