"0615-4539-39" National Drug Code (NDC)

Labetalol Hydrochloride 30 TABLET, FILM COATED in 1 BLISTER PACK (0615-4539-39)
(NCS HealthCare of KY, Inc dba Vangard Labs)

NDC Code0615-4539-39
Package Description30 TABLET, FILM COATED in 1 BLISTER PACK (0615-4539-39)
Product NDC0615-4539
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameLabetalol Hydrochloride
Non-Proprietary NameLabetalol Hydrochloride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20100114
Marketing Category NameANDA
Application NumberANDA074787
ManufacturerNCS HealthCare of KY, Inc dba Vangard Labs
Substance NameLABETALOL HYDROCHLORIDE
Strength200
Strength Unitmg/1
Pharmacy ClassesAdrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]

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