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Propranolol Hydrochloride

NDC 60687-926 · American Health Packaging

Generic namePropranolol Hydrochloride
Dosage formTABLET
RouteORAL
Active ingredient(s)PROPRANOLOL HYDROCHLORIDE
Strength10 mg/1
Pharmacologic classAdrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC]
Marketing categoryANDA

Packages

60687-926-01 — 100 BLISTER PACK in 1 CARTON (60687-926-01) / 1 TABLET in 1 BLISTER PACK (60687-926-11)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

51991-819 — propranolol hydrochloride, 51991-820 — propranolol hydrochloride, 55154-2144 — Propranolol Hydrochloride, 55154-2584 — Propranolol Hydrochloride, 55154-2646 — Propranolol Hydrochloride, 60687-215 — Propranolol Hydrochloride, 60687-226 — Propranolol Hydrochloride, 60687-587 — Propranolol Hydrochloride, 60687-598 — Propranolol Hydrochloride, 60687-609 — Propranolol Hydrochloride, 60687-937 — Propranolol Hydrochloride, 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, +184 more

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