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"10135-712-01" National Drug Code (NDC)

Labetalol Hydrochloride 100 TABLET, FILM COATED in 1 BOTTLE (10135-712-01)
(Marlex Pharmaceuticals Inc)

NDC Code10135-712-01
Package Description100 TABLET, FILM COATED in 1 BOTTLE (10135-712-01)
Product NDC10135-712
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameLabetalol Hydrochloride
Non-Proprietary NameLabetalol
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20201001
Marketing Category NameANDA
Application NumberANDA075215
ManufacturerMarlex Pharmaceuticals Inc
Substance NameLABETALOL
Strength200
Strength Unitmg/1
Pharmacy ClassesAdrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/10135-712-01





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