United States · FDA National Drug Code directory
Bupropion hydrochloride
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 47335-737_b8e6ae63-c5d7-4481-b7b0-17e135670515
- Product NDC
- 47335-737
- Form
- TABLET, FILM COATED, EXTENDED RELEASE
- Composition / generic term
- Bupropion hydrochloride
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20200301
- Source listing expiry
- 20261231
Source-listed ingredients
- BUPROPION HYDROCHLORIDE — 150 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (47335-737-08) · 47335-737-08
- 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (47335-737-13) · 47335-737-13
- 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (47335-737-86) · 47335-737-86
- 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (47335-737-88) · 47335-737-88
Source and coverage
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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
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