# Bupropion Hydrochloride (XL)

NDC: 43598-656
Generic name: bupropion hydrochloride
Labeler / Manufacturer: Dr Reddys Laboratories Inc
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20170412

FDA application: ANDA207479

## 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:"43598-656"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=43598-656
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=d5469d64-5e74-4b7a-b4cd-551665f6adaa