"61919-332-90" National Drug Code (NDC)

Lisinopril 90 TABLET in 1 BOTTLE (61919-332-90)
(DirectRX)

NDC Code61919-332-90
Package Description90 TABLET in 1 BOTTLE (61919-332-90)
Product NDC61919-332
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameLisinopril
Non-Proprietary NameLisinopril
Dosage FormTABLET
UsageORAL
Start Marketing Date20150101
Marketing Category NameANDA
Application NumberANDA202554
ManufacturerDirectRX
Substance NameLISINOPRIL
Strength5
Strength Unitmg/1
Pharmacy ClassesAngiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA]

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