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
- 71610-899_59d3655a-a828-6c81-e063-6294a90ac103
- Product NDC
- 71610-899
- Form
- TABLET
- Composition / generic term
- Bupropion Hydrochloride
- Labeler
- Aphena Pharma Solutions - Tennessee, LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20250130
- Source listing expiry
- 20271231
Source-listed ingredients
- BUPROPION HYDROCHLORIDE — 75 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1800 TABLET in 1 BOTTLE (71610-899-42) · 71610-899-42
- 60 TABLET in 1 BOTTLE (71610-899-53) · 71610-899-53
- 90 TABLET in 1 BOTTLE (71610-899-60) · 71610-899-60
- 180 TABLET in 1 BOTTLE (71610-899-80) · 71610-899-80
Source and coverage
Open FDA National Drug Code directory →
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.
Browse United States records →