Skip to main content

Nebivolol

NDC 31722-588 · Camber Pharmaceuticals, Inc.

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

Packages

31722-588-01 — 100 TABLET in 1 BOTTLE (31722-588-01)

31722-588-30 — 30 TABLET in 1 BOTTLE (31722-588-30)

31722-588-32 — 10 BLISTER PACK in 1 CARTON (31722-588-32) / 10 TABLET in 1 BLISTER PACK (31722-588-31)

31722-588-34 — 18 BLISTER PACK in 1 CARTON (31722-588-34) / 7 TABLET in 1 BLISTER PACK (31722-588-33)

31722-588-90 — 90 TABLET in 1 BOTTLE (31722-588-90)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

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, 31722-585 — Nebivolol, 31722-586 — Nebivolol, 31722-587 — 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, 42291-874 — nebivolol hydrochloride, 50090-5708 — Nebivolol, 50090-5752 — Nebivolol, +62 more

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