# Bupropion Hydrochloride XL

NDC: 70436-010
Generic name: bupropion hydrochloride
Labeler / Manufacturer: Slate Run Pharmaceuticals, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20181201

FDA application: ANDA210015

## Active ingredients

- BUPROPION HYDROCHLORIDE: 150 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"70436-010"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70436-010
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=06d4d890-11ed-4f31-8778-c73432e3ea69