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
64380-269_c59340fa-0b07-454a-bf5a-c49b54bfd42c
Product NDC
64380-269
Form
TABLET, FILM COATED
Composition / generic term
PROPAFENONE HYDROCHLORIDE
Labeler
Strides Pharma Science Limited
Marketing category
ANDA
Marketing start / end (source format)
20250505
Source listing expiry
20271231

Source-listed ingredients

  • PROPAFENONE HYDROCHLORIDE — 150 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 300 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (64380-269-01) · 64380-269-01
  • 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (64380-269-02) · 64380-269-02

Source and coverage

Open FDA National Drug Code directory

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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PROPAFENONE HYDROCHLORIDE — United States | Molindra Medicines