# PRAVASTATIN SODIUM

NDC: 68180-486
Generic name: PRAVASTATIN SODIUM
Labeler / Manufacturer: Lupin Pharmaceuticals, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20080724

FDA application: ANDA077917

## 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:"68180-486"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68180-486
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=1123d56c-16f0-4f81-b56f-67b1f343ae1e