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
- 69292-602_3e54a2cc-6e29-482c-a6ee-451b3a1a15f3
- Product NDC
- 69292-602
- Form
- TABLET, FILM COATED
- Composition / generic term
- Bupropion Hydrochloride
- Labeler
- Amici Pharma, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20260521
- Source listing expiry
- 20271231
Source-listed ingredients
- BUPROPION HYDROCHLORIDE — 100 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET, FILM COATED in 1 BOTTLE (69292-602-01) · 69292-602-01
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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