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Propranolol Hydrochloride

NDC 71335-0955 · Bryant Ranch Prepack

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

Packages

71335-0955-1 — 30 TABLET in 1 BOTTLE (71335-0955-1)

71335-0955-2 — 100 TABLET in 1 BOTTLE (71335-0955-2)

71335-0955-3 — 90 TABLET in 1 BOTTLE (71335-0955-3)

71335-0955-4 — 60 TABLET in 1 BOTTLE (71335-0955-4)

71335-0955-5 — 10 TABLET in 1 BOTTLE (71335-0955-5)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

70756-298 — Propranolol hydrochloride, 71205-446 — Propranolol Hydrochloride, 71205-590 — Propranolol Hydrochloride, 71205-760 — Propranolol Hydrochloride, 71205-761 — Propranolol Hydrochloride, 71205-794 — Propranolol Hydrochloride, 71335-0082 — propranolol hydrochloride, 71335-0234 — propranolol hydrochloride, 71335-0472 — propranolol hydrochloride, 71335-0554 — propranolol hydrochloride, 71335-1712 — Propranolol Hydrochloride, 71335-1765 — propranolol hydrochloride, 71335-1994 — Propranolol Hydrochloride, 71335-2299 — propranolol hydrochloride, 71335-2315 — propranolol hydrochloride, 71335-2369 — Propranolol Hydrochloride, 71335-2371 — Propranolol Hydrochloride, 71335-2372 — Propranolol Hydrochloride, 71335-2594 — Propranolol hydrochloride, 71335-2781 — 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.