NDC 69238-2081 – Propranolol Hydrochloride

Propranolol Hydrochloride 80 mg/1 · Tablet · Oral

Human Prescription Drug 1 recall

Product NDC69238-2081

Product details

Brand name
Propranolol Hydrochloride
Generic name
Propranolol Hydrochloride
Labeler
Amneal Pharmaceuticals NY LLC
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA071976
Marketed since
June 3, 2021
Listing expires
December 31, 2027
Pharmacologic class
beta-Adrenergic Blocker

Active ingredients

Uses, dosage, side effects and warnings for Propranolol Hydrochloride →

Package NDC codes (2)

Package NDCDescriptionSince
69238-2081-1100 TABLET in 1 BOTTLE (69238-2081-1)Jun 3, 2021
69238-2081-5500 TABLET in 1 BOTTLE (69238-2081-5)Jun 3, 2021

Recalls mentioning this NDC

Other Propranolol Hydrochloride products