United States · FDA National Drug Code directory
Bupropion HCL ER(SR)
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
- 72189-676_5a5c4d58-a185-a95d-e063-6394a90a0b7e
- Product NDC
- 72189-676
- Form
- TABLET, EXTENDED RELEASE
- Composition / generic term
- Bupropion HCL ER(SR)
- Labeler
- DriectRx
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20260430
- Source listing expiry
- 20271231
Source-listed ingredients
- BUPROPION HYDROCHLORIDE — 100 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (72189-676-30) · 72189-676-30
- 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (72189-676-60) · 72189-676-60
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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