"29300-254-05" National Drug Code (NDC)

Labetalol Hydrochloride 500 TABLET, FILM COATED in 1 BOTTLE (29300-254-05)
(Unichem Pharmaceuticals (USA), Inc.)

NDC Code29300-254-05
Package Description500 TABLET, FILM COATED in 1 BOTTLE (29300-254-05)
Product NDC29300-254
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
Strength300
Strength Unitmg/1
Pharmacy ClassesAdrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC]

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