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"23155-725-01" National Drug Code (NDC)

Labetalol Hydrochloride 100 TABLET in 1 BOTTLE (23155-725-01)
(Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.)

NDC Code23155-725-01
Package Description100 TABLET in 1 BOTTLE (23155-725-01)
Product NDC23155-725
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
Strength300
Strength Unitmg/1
Pharmacy ClassesAdrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/23155-725-01





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