"16590-994-30" National Drug Code (NDC)

Labetalol Hydrochloride 30 TABLET, FILM COATED in 1 BOTTLE (16590-994-30)
(STAT RX USA LLC)

NDC Code16590-994-30
Package Description30 TABLET, FILM COATED in 1 BOTTLE (16590-994-30)
Product NDC16590-994
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameLabetalol Hydrochloride
Non-Proprietary NameLabetalol Hydrochloride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date19980803
Marketing Category NameANDA
Application NumberANDA075133
ManufacturerSTAT RX USA LLC
Substance NameLABETALOL HYDROCHLORIDE
Strength300
Strength Unitmg/1
Pharmacy ClassesAdrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]

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