"29300-252-01" National Drug Code (NDC)

Labetalol Hydrochloride 100 TABLET, FILM COATED in 1 BOTTLE (29300-252-01)
(Unichem Pharmaceuticals (USA), Inc.)

NDC Code29300-252-01
Package Description100 TABLET, FILM COATED in 1 BOTTLE (29300-252-01)
Product NDC29300-252
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameLabetalol Hydrochloride
Non-Proprietary NameLabetalol Hydrochloride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20221001
Marketing Category NameANDA
Application NumberANDA212719
ManufacturerUnichem Pharmaceuticals (USA), Inc.
Substance NameLABETALOL HYDROCHLORIDE
Strength100
Strength Unitmg/1
Pharmacy ClassesAdrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/29300-252-01