"0904-5929-61" National Drug Code (NDC)

Labetalol Hydrochloride 100 BLISTER PACK in 1 CARTON (0904-5929-61) > 1 TABLET, FILM COATED in 1 BLISTER PACK
(Major Pharmaceuticals)

NDC Code0904-5929-61
Package Description100 BLISTER PACK in 1 CARTON (0904-5929-61) > 1 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC0904-5929
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameLabetalol Hydrochloride
Non-Proprietary NameLabetalol Hydrochloride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20090610
End Marketing Date20211231
Marketing Category NameANDA
Application NumberANDA075133
ManufacturerMajor Pharmaceuticals
Substance NameLABETALOL HYDROCHLORIDE
Strength200
Strength Unitmg/1
Pharmacy ClassesAdrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]

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