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Propranolol Hydrochloride

NDC 62559-531 · ANI Pharmaceuticals, Inc.

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 categoryNDA AUTHORIZED GENERIC

Packages

62559-531-01 — 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (62559-531-01)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

60687-948 — Propranolol Hydrochloride, 60760-545 — Propranolol Hydrochloride, 60760-589 — propranolol hydrochloride, 60760-731 — Propranolol Hydrochloride, 60760-867 — propranolol hydrochloride, 62559-520 — propranolol hydrochloride, 62559-521 — propranolol hydrochloride, 62559-522 — propranolol hydrochloride, 62559-523 — propranolol hydrochloride, 62559-530 — propranolol hydrochloride, 62559-532 — propranolol hydrochloride, 62559-533 — propranolol hydrochloride, 62559-590 — propranolol hydrochloride, 62559-591 — propranolol hydrochloride, 62559-600 — propranolol hydrochloride, 62559-601 — propranolol hydrochloride, 63323-604 — PROPRANOLOL HYDROCHLORIDE, 63629-2069 — propranolol hydrochloride, 63629-2070 — propranolol hydrochloride, 63629-2071 — 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.