"60687-136-01" National Drug Code (NDC)

Labetalol Hcl 100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-136-01) > 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-136-11)
(American Health Packaging)

NDC Code60687-136-01
Package Description100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-136-01) > 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-136-11)
Product NDC60687-136
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameLabetalol Hcl
Non-Proprietary NameLabetalol Hcl
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20150930
End Marketing Date20200831
Marketing Category NameANDA
Application NumberANDA075113
ManufacturerAmerican Health Packaging
Substance NameLABETALOL HYDROCHLORIDE
Strength300
Strength Unitmg/1
Pharmacy ClassesAdrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]

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