# Nevirapine

NDC: 65862-057
Generic name: Nevirapine
Labeler / Manufacturer: Aurobindo Pharma Limited
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SUSPENSION
Routes: ORAL
Marketing started: 20120522

FDA application: ANDA077702

## Active ingredients

- NEVIRAPINE HEMIHYDRATE: 50 mg/5mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"65862-057"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=65862-057
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=8dfe86aa-ea5d-48d2-94a8-1a5506055d70