United States · FDA National Drug Code directory
bupropion hydrochloride SR
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
- 43547-288_9424dd2e-19ad-4f3d-b533-ba504a18ff77
- Product NDC
- 43547-288
- Form
- TABLET, FILM COATED, EXTENDED RELEASE
- Composition / generic term
- Bupropion hydrochloride
- Labeler
- Solco Healthcare US LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20141101
- Source listing expiry
- 20271231
Source-listed ingredients
- BUPROPION HYDROCHLORIDE — 100 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (43547-288-06) · 43547-288-06
- 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (43547-288-09) · 43547-288-09
- 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (43547-288-10) · 43547-288-10
- 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (43547-288-50) · 43547-288-50
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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