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"71209-085-03" National Drug Code (NDC)

Labetalol Hydrochloride 60 TABLET, FILM COATED in 1 BOTTLE (71209-085-03)
(Cadila Pharmaceuticals Limited)

NDC Code71209-085-03
Package Description60 TABLET, FILM COATED in 1 BOTTLE (71209-085-03)
Product NDC71209-085
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameLabetalol Hydrochloride
Non-Proprietary NameLabetalol Hydrochloride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20180305
Marketing Category NameANDA
Application NumberANDA211325
ManufacturerCadila Pharmaceuticals Limited
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/71209-085-03





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