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"0172-4364-10" National Drug Code (NDC)

Labetalol Hydrochloride 100 BLISTER PACK in 1 BOX, UNIT-DOSE (0172-4364-10) > 1 TABLET, FILM COATED in 1 BLISTER PACK (0172-4364-00)
(IVAX Pharmaceuticals, Inc.)

NDC Code0172-4364-10
Package Description100 BLISTER PACK in 1 BOX, UNIT-DOSE (0172-4364-10) > 1 TABLET, FILM COATED in 1 BLISTER PACK (0172-4364-00)
Product NDC0172-4364
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameLabetalol Hydrochloride
Non-Proprietary NameLabetalol Hydrochloride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date19980803
Marketing Category NameANDA
Application NumberANDA074787
ManufacturerIVAX Pharmaceuticals, Inc.
Substance NameLABETALOL HYDROCHLORIDE
Strength100
Strength Unitmg/1
Pharmacy ClassesAdrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]

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