NDC 68788-8595 – Propranolol Hydrochloride

Propranolol Hydrochloride 20 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC68788-8595

Product details

Brand name
Propranolol Hydrochloride
Generic name
Propranolol Hydrochloride
Labeler
Preferred Pharmaceuticals Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA071972
Marketed since
March 1, 2024
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
68788-8595-330 TABLET in 1 BOTTLE (68788-8595-3)Mar 1, 2024
68788-8595-990 TABLET in 1 BOTTLE (68788-8595-9)Mar 1, 2024

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