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Propranolol Hydrochloride

NDC 0603-5484 · Endo USA, Inc.

Generic namepropranolol hydrochloride
Dosage formTABLET
RouteORAL
Active ingredient(s)PROPRANOLOL HYDROCHLORIDE
Strength40 mg/1
Pharmacologic classAdrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC]
Marketing categoryANDA

Packages

0603-5484-21 — 100 TABLET in 1 BOTTLE (0603-5484-21)

0603-5484-32 — 1000 TABLET in 1 BOTTLE (0603-5484-32)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

0378-0184 — propranolol hydrochloride, 0378-0185 — propranolol hydrochloride, 0378-0187 — propranolol hydrochloride, 0404-9999 — propranolol hydrochloride, 0527-4116 — propranolol hydrochloride, 0527-4117 — propranolol hydrochloride, 0527-4118 — propranolol hydrochloride, 0527-4119 — propranolol hydrochloride, 0603-5482 — propranolol hydrochloride, 0603-5483 — propranolol hydrochloride, 0603-5485 — propranolol hydrochloride, 0603-5486 — propranolol hydrochloride, 0615-8413 — Propranolol Hydrochloride, 0615-8417 — Propranolol Hydrochloride, 0615-8426 — Propranolol Hydrochloride, 0904-7467 — Propranolol Hydrochloride, 0904-7468 — Propranolol Hydrochloride, 17856-3728 — Propranolol Hydrochloride, 17856-8728 — Propranolol Hydrochloride, 42291-522 — propranolol hydrochloride, +184 more

From the FDA National Drug Code Directory, retrieved August 24, 2026. Product listings are submitted by labelers; FDA does not verify them.