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
- 71209-053_fff2e22d-64c2-425f-823f-a34664d4b1aa
- Product NDC
- 71209-053
- Form
- TABLET, FILM COATED
- Composition / generic term
- Bupropion Hydrochloride
- Labeler
- Cadila Pharmaceuticals Limited
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20200116
- 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 (71209-053-05) · 71209-053-05
- 1000 TABLET, FILM COATED in 1 BOTTLE (71209-053-11) · 71209-053-11
- 10 BLISTER PACK in 1 CARTON (71209-053-17) / 10 TABLET, FILM COATED in 1 BLISTER PACK · 71209-053-17
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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