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
- 71335-1214_6c94f0d8-1b25-4963-9368-2a632fa8348c
- Product NDC
- 71335-1214
- Form
- TABLET, EXTENDED RELEASE
- Composition / generic term
- BUPROPION HYDROCHLORIDE
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20190325
- Source listing expiry
- 20271231
Source-listed ingredients
- BUPROPION HYDROCHLORIDE — 300 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1214-1) · 71335-1214-1
- 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1214-2) · 71335-1214-2
- 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1214-3) · 71335-1214-3
- 120 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1214-4) · 71335-1214-4
- 8 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1214-5) · 71335-1214-5
- 180 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1214-6) · 71335-1214-6
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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