NDC 16571-736 – Propafenone Hydrochloride

Propafenone Hydrochloride 225 mg/1 · Capsule, Extended Release · Oral

Human Prescription Drug

Product NDC16571-736

Product details

Brand name
Propafenone Hydrochloride
Generic name
Propafenone Hydrochloride
Labeler
Rising Pharma Holdings, Inc.
Dosage form
Capsule, Extended Release
Route
Oral
Marketing category
ANDA · ANDA205956
Marketed since
December 16, 2020
Listing expires
December 31, 2026
Pharmacologic class
Antiarrhythmic

Active ingredients

Uses, dosage, side effects and warnings for Propafenone hydrochloride →

Package NDC codes (2)

Package NDCDescriptionSince
16571-736-0660 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (16571-736-06)Dec 16, 2020
16571-736-50500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (16571-736-50)Dec 16, 2020

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