# buPropion Hydrochloride XL

NDC: 72516-036
Generic name: bupropion hydrochloride
Labeler / Manufacturer: Oryza pharmaceuticals Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20190906

FDA application: ANDA211200

## Active ingredients

- BUPROPION HYDROCHLORIDE: 300 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"72516-036"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=72516-036
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=004d8121-59d4-46c4-acb8-b2dd097bf556