United States · FDA National Drug Code directory
Bupropion Hydrochloride (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
- 43598-656_dc27d1dd-5931-08dc-e053-2995a90a21f0
- Product NDC
- 43598-656
- Form
- TABLET, FILM COATED, EXTENDED RELEASE
- Composition / generic term
- bupropion hydrochloride
- Labeler
- Dr Reddys Laboratories Inc
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20170412
- Source listing expiry
- 20261231
Source-listed ingredients
- BUPROPION HYDROCHLORIDE — 300 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (43598-656-05) · 43598-656-05
- 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (43598-656-30) · 43598-656-30
- 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (43598-656-90) · 43598-656-90
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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