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
- 64380-164_3c3e948d-7eef-4a8b-8155-aef063cd1678
- Product NDC
- 64380-164
- Form
- TABLET, FILM COATED
- Composition / generic term
- PROPAFENONE HYDROCHLORIDE
- Labeler
- Strides Pharma Science Limited
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20220801
- Source listing expiry
- 20261231
Source-listed ingredients
- PROPAFENONE HYDROCHLORIDE — 225 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 300 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (64380-164-01) · 64380-164-01
- 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (64380-164-02) · 64380-164-02
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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