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"69097-839-15" National Drug Code (NDC)

Quinapril 1000 TABLET in 1 BOTTLE (69097-839-15)
(Cipla USA Inc.)

NDC Code69097-839-15
Package Description1000 TABLET in 1 BOTTLE (69097-839-15)
Product NDC69097-839
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameQuinapril
Non-Proprietary NameQuinapril
Dosage FormTABLET
UsageORAL
Start Marketing Date20160722
Marketing Category NameANDA
Application NumberANDA078457
ManufacturerCipla USA Inc.
Substance NameQUINAPRIL HYDROCHLORIDE
Strength5
Strength Unitmg/1
Pharmacy ClassesAngiotensin Converting Enzyme Inhibitor [EPC], Angiotensin-converting Enzyme Inhibitors [MoA]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/69097-839-15





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