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
- 60505-0157_9d602b2e-4f88-650d-f47e-d63fb7aacf92
- Product NDC
- 60505-0157
- Form
- TABLET, FILM COATED
- Composition / generic term
- Bupropion Hydrochloride
- Labeler
- Apotex Corp
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20060117
- 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 (60505-0157-1) · 60505-0157-1
- 30 TABLET, FILM COATED in 1 BOTTLE (60505-0157-3) · 60505-0157-3
- 500 TABLET, FILM COATED in 1 BOTTLE (60505-0157-5) · 60505-0157-5
- 1000 TABLET, FILM COATED in 1 BOTTLE (60505-0157-7) · 60505-0157-7
- 90 TABLET, FILM COATED in 1 BOTTLE (60505-0157-9) · 60505-0157-9
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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