Nebivolol

NDC 31722-585 · Camber Pharmaceuticals, Inc.

Generic nameNebivolol

Dosage formTABLET

RouteORAL

Active ingredient(s)NEBIVOLOL HYDROCHLORIDE

Strength2.5 mg/1

Pharmacologic classAdrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC]

Marketing categoryANDA

Packages

31722-585-01 — 100 TABLET in 1 BOTTLE (31722-585-01)

31722-585-30 — 30 TABLET in 1 BOTTLE (31722-585-30)

31722-585-32 — 12 BLISTER PACK in 1 CARTON (31722-585-32) / 10 TABLET in 1 BLISTER PACK (31722-585-31)

31722-585-34 — 15 BLISTER PACK in 1 CARTON (31722-585-34) / 10 TABLET in 1 BLISTER PACK (31722-585-33)

FDA lists these products with the same active ingredient.

0456-1410 — nebivolol hydrochloride, 0456-1420 — nebivolol hydrochloride, 24689-159 — nebivolol hydrochloride, 24689-160 — nebivolol hydrochloride, 24689-161 — nebivolol hydrochloride, 24689-162 — nebivolol hydrochloride, 29300-375 — Nebivolol Hydrochloride, 29300-376 — Nebivolol Hydrochloride, 29300-377 — Nebivolol Hydrochloride, 29300-378 — Nebivolol Hydrochloride, 31722-586 — Nebivolol, 31722-587 — Nebivolol, 31722-588 — Nebivolol, 33342-457 — Nebivolol, 33342-458 — Nebivolol, 33342-459 — Nebivolol, 33342-460 — Nebivolol, 42291-871 — nebivolol hydrochloride, 42291-872 — nebivolol hydrochloride, 42291-873 — nebivolol hydrochloride, +62 more

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