NDC 16714-826 – Propafenone hydrochloride

Propafenone Hydrochloride 325 mg/1 · Capsule, Extended Release · Oral

Human Prescription Drug 2 recalls

Product NDC16714-826

Product details

Brand name
Propafenone hydrochloride
Generic name
Propafenone hydrochloride
Labeler
Northstar Rx LLC
Dosage form
Capsule, Extended Release
Route
Oral
Marketing category
ANDA · ANDA205268
Marketed since
March 31, 2017
Listing expires
December 31, 2027
Pharmacologic class
Antiarrhythmic

Active ingredients

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

Package NDC codes (1)

Package NDCDescriptionSince
16714-826-0160 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (16714-826-01)Jul 16, 2018

Recalls mentioning this NDC

Other Propafenone hydrochloride products