"68001-332-03" National Drug Code (NDC)

Lisinopril 500 TABLET in 1 BOTTLE (68001-332-03)
(BluePoint Laboratories)

NDC Code68001-332-03
Package Description500 TABLET in 1 BOTTLE (68001-332-03)
Product NDC68001-332
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameLisinopril
Non-Proprietary NameLisinopril
Dosage FormTABLET
UsageORAL
Start Marketing Date20170801
Marketing Category NameANDA
Application NumberANDA077321
ManufacturerBluePoint Laboratories
Substance NameLISINOPRIL
Strength2.5
Strength Unitmg/1
Pharmacy ClassesAngiotensin Converting Enzyme Inhibitor [EPC], Angiotensin-converting Enzyme Inhibitors [MoA]

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