NDC 51655-302 – Propranolol Hydrochloride

Propranolol Hydrochloride 20 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC51655-302

Product details

Brand name
Propranolol Hydrochloride
Generic name
Propranolol hydrochloride
Labeler
Northwind Health Company, LLC
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA070221
Marketed since
May 19, 2020
Listing expires
December 31, 2027
Pharmacologic class
beta-Adrenergic Blocker

Active ingredients

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

Package NDC codes (1)

Package NDCDescriptionSince
51655-302-2690 TABLET in 1 BOTTLE, PLASTIC (51655-302-26)May 19, 2020

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