"65862-619-19" National Drug Code (NDC)

Quinapril 10000 TABLET, FILM COATED in 1 BOTTLE (65862-619-19)
(Aurobindo Pharma Limited)

NDC Code65862-619-19
Package Description10000 TABLET, FILM COATED in 1 BOTTLE (65862-619-19)
Product NDC65862-619
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameQuinapril
Non-Proprietary NameQuinapril Hydrochloride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20130429
Marketing Category NameANDA
Application NumberANDA202725
ManufacturerAurobindo Pharma Limited
Substance NameQUINAPRIL HYDROCHLORIDE
Strength20
Strength Unitmg/1
Pharmacy ClassesAngiotensin Converting Enzyme Inhibitor [EPC], Angiotensin-converting Enzyme Inhibitors [MoA]

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