# Pravastatin Sodium

NDC: 35356-919
Generic name: pravastatin sodium
Labeler / Manufacturer: Lake Erie Medical DBA Quality Care Products LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20110718
Marketing ended: 20280430
FDA application: ANDA076341

## 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:"35356-919"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=35356-919
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=e7194af1-6304-4e3e-88ab-0825706a3962