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
- 42806-410_af1a3522-8180-4e3f-a2fc-c9fe143997a3
- Product NDC
- 42806-410
- Form
- TABLET, EXTENDED RELEASE
- Composition / generic term
- BUPROPION HYDROCHLORIDE
- Labeler
- Epic Pharma LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20211215
- Source listing expiry
- 20261231
Source-listed ingredients
- BUPROPION HYDROCHLORIDE — 100 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (42806-410-01) · 42806-410-01
- 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (42806-410-05) · 42806-410-05
- 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (42806-410-60) · 42806-410-60
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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