# Nevirapine

NDC: 0378-4050
Generic name: nevirapine
Labeler / Manufacturer: Mylan Pharmaceuticals Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20120522

FDA application: ANDA202523

## Active ingredients

- NEVIRAPINE: 200 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0378-4050"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0378-4050
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=c6e93829-7024-48f6-8023-da6ff27dfc0a