"58657-908-01" National Drug Code (NDC)

Labetalol Hydrochloride 100 BLISTER PACK in 1 CARTON (58657-908-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (58657-908-10)
(Method Pharmaceuticals, LLC)

NDC Code58657-908-01
Package Description100 BLISTER PACK in 1 CARTON (58657-908-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (58657-908-10)
Product NDC58657-908
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameLabetalol Hydrochloride
Non-Proprietary NameLabetalol Hydrochloride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20250701
Marketing Category NameANDA
Application NumberANDA075215
ManufacturerMethod Pharmaceuticals, LLC
Substance NameLABETALOL
Strength300
Strength Unitmg/1
Pharmacy ClassesAdrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC]

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