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: 72241-020_fe5a706a-47cf-47d4-a6ed-db4e7f08a169
Product NDC: 72241-020
Form: TABLET, FILM COATED
Composition / generic term: Bupropion Hydrochloride
Labeler: Modavar Pharmaceuticals LLC
Marketing category: ANDA
Marketing start / end (source format): 20200116
Source listing expiry: 20261231

Source-listed ingredients

BUPROPION HYDROCHLORIDE — 75 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

100 TABLET, FILM COATED in 1 BOTTLE (72241-020-05) · 72241-020-05
1000 TABLET, FILM COATED in 1 BOTTLE (72241-020-11) · 72241-020-11
10 BLISTER PACK in 1 CARTON (72241-020-17) / 10 TABLET, FILM COATED in 1 BLISTER PACK · 72241-020-17

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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