# Bupropion Hydrochloride

NDC: 24689-119
Generic name: Bupropion Hydrochloride
Labeler / Manufacturer: Apnar Pharma LP
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20211220

FDA application: ANDA075584

## Active ingredients

- BUPROPION HYDROCHLORIDE: 75 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"24689-119"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=24689-119
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=d1830cfd-e7f4-345c-e053-2995a90a2251