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"0615-7688-39" National Drug Code (NDC)

Labetalol Hydrochloride 30 TABLET, FILM COATED in 1 BLISTER PACK (0615-7688-39)
(NCS HealthCare of KY, Inc dba Vangard Labs)

NDC Code0615-7688-39
Package Description30 TABLET, FILM COATED in 1 BLISTER PACK (0615-7688-39)
Product NDC0615-7688
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameLabetalol Hydrochloride
Non-Proprietary NameLabetalol Hydrochloride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20110101
Marketing Category NameANDA
Application NumberANDA074787
ManufacturerNCS HealthCare of KY, Inc dba Vangard Labs
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/0615-7688-39





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