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Propranolol Hydrochloride

NDC 67046-1582 · Coupler LLC

Generic namePropranolol Hydrochloride
Dosage formTABLET
RouteORAL
Active ingredient(s)PROPRANOLOL HYDROCHLORIDE
Strength60 mg/1
Pharmacologic classAdrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC]
Marketing categoryANDA

Packages

67046-1582-3 — 30 TABLET in 1 BLISTER PACK (67046-1582-3)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

63629-2278 — propranolol hydrochloride, 63629-2279 — propranolol hydrochloride, 63629-2280 — propranolol hydrochloride, 63629-2281 — propranolol hydrochloride, 63629-2282 — propranolol hydrochloride, 63629-9282 — propranolol hydrochloride, 63629-9953 — propranolol hydrochloride, 64370-375 — propranolol hydrochloride, 66267-261 — propranolol hydrochloride, 67046-0211 — Propranolol Hydrochloride, 67046-1657 — Propranolol Hydrochloride, 68071-2710 — Propranolol Hydrochloride, 68071-3576 — Propranolol Hydrochloride, 68071-5071 — propranolol hydrochloride, 68788-4089 — Propranolol Hydrochloride, 68788-4131 — Propranolol Hydrochloride, 68788-7791 — Propranolol Hydrochloride, 68788-7860 — Propranolol Hydrochloride, 68788-8595 — Propranolol Hydrochloride, 68788-8604 — 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.