United States · FDA National Drug Code directory
Propafenone 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
- 71335-2780_8091654a-d552-41b3-b090-2ae99ef6dee3
- Product NDC
- 71335-2780
- Form
- TABLET, COATED
- Composition / generic term
- Propafenone Hydrochloride
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20150331
- Source listing expiry
- 20261231
Source-listed ingredients
- PROPAFENONE HYDROCHLORIDE — 150 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 TABLET, COATED in 1 BOTTLE (71335-2780-1) · 71335-2780-1
- 90 TABLET, COATED in 1 BOTTLE (71335-2780-2) · 71335-2780-2
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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