"58657-602-50" National Drug Code (NDC)

Labetalol Hydrochloride 500 TABLET, FILM COATED in 1 BOTTLE (58657-602-50)
(Method Pharmaceuticals, LLC)

NDC Code58657-602-50
Package Description500 TABLET, FILM COATED in 1 BOTTLE (58657-602-50)
Product NDC58657-602
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameLabetalol Hydrochloride
Non-Proprietary NameLabetalol Hydrochloride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20191122
Marketing Category NameANDA
Application NumberANDA075215
ManufacturerMethod Pharmaceuticals, LLC
Substance NameLABETALOL
Strength100
Strength Unitmg/1
Pharmacy ClassesAdrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC]

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