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Propranolol Hydrochloride

NDC 50090-7620 · A-S Medication Solutions

Generic namePropranolol Hydrochloride
Dosage formTABLET
RouteORAL
Active ingredient(s)PROPRANOLOL HYDROCHLORIDE
Strength20 mg/1
Pharmacologic classAdrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC]
Marketing categoryANDA

Packages

50090-7620-0 — 30 TABLET in 1 BOTTLE (50090-7620-0)

50090-7620-1 — 100 TABLET in 1 BOTTLE (50090-7620-1)

50090-7620-6 — 90 TABLET in 1 BOTTLE (50090-7620-6)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

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, 50090-7618 — Propranolol Hydrochloride, 50268-662 — Propranolol Hydrochloride, 50268-663 — Propranolol Hydrochloride, 50268-664 — Propranolol Hydrochloride, 51407-235 — propranolol hydrochloride, 51407-236 — propranolol hydrochloride, 51407-237 — propranolol hydrochloride, 51407-238 — propranolol hydrochloride, 51407-239 — propranolol hydrochloride, 51655-228 — Propranolol Hydrochloride, 51655-302 — 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.