"68180-763-03" National Drug Code (NDC)

Nadolol 1000 TABLET in 1 BOTTLE (68180-763-03)
(Lupin Pharmaceuticals, Inc.)

NDC Code68180-763-03
Package Description1000 TABLET in 1 BOTTLE (68180-763-03)
Product NDC68180-763
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameNadolol
Non-Proprietary NameNadolol
Dosage FormTABLET
UsageORAL
Start Marketing Date20171005
Marketing Category NameANDA
Application NumberANDA209309
ManufacturerLupin Pharmaceuticals, Inc.
Substance NameNADOLOL
Strength80
Strength Unitmg/1
Pharmacy ClassesAdrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]

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