"23155-723-01" National Drug Code (NDC)

Labetalol Hydrochloride 100 TABLET in 1 BOTTLE (23155-723-01)
(Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.)

NDC Code23155-723-01
Package Description100 TABLET in 1 BOTTLE (23155-723-01)
Product NDC23155-723
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameLabetalol Hydrochloride
Non-Proprietary NameLabetalol Hydrochloride
Dosage FormTABLET
UsageORAL
Start Marketing Date20200222
Marketing Category NameANDA
Application NumberANDA074787
ManufacturerHeritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.
Substance NameLABETALOL HYDROCHLORIDE
Strength100
Strength Unitmg/1
Pharmacy ClassesAdrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC]

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