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
- 71205-504_8ab86beb-3616-414c-92bf-25273a853a9e
- Product NDC
- 71205-504
- Form
- TABLET, EXTENDED RELEASE
- Composition / generic term
- BUPROPION HYDROCHLORIDE
- Labeler
- Proficient Rx LP
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20181108
- Source listing expiry
- 20261231
Source-listed ingredients
- BUPROPION HYDROCHLORIDE — 150 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-504-30) · 71205-504-30
- 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-504-60) · 71205-504-60
- 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-504-90) · 71205-504-90
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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