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"68084-129-01" National Drug Code (NDC)

Labetalol Hydrochloride 10 BLISTER PACK in 1 CARTON (68084-129-01) > 10 TABLET, FILM COATED in 1 BLISTER PACK (68084-129-11)
(American Health Packaging)

NDC Code68084-129-01
Package Description10 BLISTER PACK in 1 CARTON (68084-129-01) > 10 TABLET, FILM COATED in 1 BLISTER PACK (68084-129-11)
Product NDC68084-129
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameLabetalol Hydrochloride
Non-Proprietary NameLabetalol Hydrochloride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20110308
Marketing Category NameANDA
Application NumberANDA075133
ManufacturerAmerican Health Packaging
Substance NameLABETALOL HYDROCHLORIDE
Strength100
Strength Unitmg/1
Pharmacy ClassesAdrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/68084-129-01





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