NDC 68462-408 – Propafenone hydrochloride

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

Human Prescription Drug 2 recalls

Product NDC68462-408

Product details

Brand name
Propafenone hydrochloride
Generic name
Propafenone hydrochloride
Labeler
Glenmark Pharmaceuticals Inc., USA
Dosage form
Capsule, Extended Release
Route
Oral
Marketing category
ANDA · ANDA205268
Marketed since
September 8, 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
68462-408-6060 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68462-408-60)Sep 8, 2017

Recalls mentioning this NDC

Other Propafenone hydrochloride products