United States · FDA National Drug Code directory
WELLBUTRIN XL
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
- 0187-0730_22308f71-fc56-430d-b559-bed47e17a46c
- Product NDC
- 0187-0730
- Form
- TABLET, EXTENDED RELEASE
- Composition / generic term
- bupropion hydrochloride
- Labeler
- Bausch Health US LLC
- Marketing category
- NDA
- Marketing start / end (source format)
- 20030829
- Source listing expiry
- 20271231
Source-listed ingredients
- BUPROPION HYDROCHLORIDE — 150 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 7 TABLET, EXTENDED RELEASE in 1 BOTTLE (0187-0730-07) · 0187-0730-07
- 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (0187-0730-30) · 0187-0730-30
- 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (0187-0730-90) · 0187-0730-90
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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