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propranolol hydrochloride

NDC 42291-523 · AvKARE

Generic namepropranolol hydrochloride
Dosage formCAPSULE, EXTENDED RELEASE
RouteORAL
Active ingredient(s)PROPRANOLOL HYDROCHLORIDE
Strength80 mg/1
Pharmacologic classAdrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC]
Marketing categoryANDA

Packages

42291-523-01 — 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (42291-523-01)

42291-523-10 — 1000 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (42291-523-10)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

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, 42291-524 — propranolol hydrochloride, 42291-525 — propranolol hydrochloride, 43063-647 — propranolol hydrochloride, 43353-961 — propranolol hydrochloride, 50090-1501 — propranolol hydrochloride, 50090-7097 — Propranolol Hydrochloride, 50090-7101 — Propranolol Hydrochloride, 50090-7104 — Propranolol Hydrochloride, 50090-7263 — propranolol hydrochloride, 50090-7593 — 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.