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"69097-842-15" National Drug Code (NDC)
Quinapril 1000 TABLET in 1 BOTTLE (69097-842-15)
(Cipla USA Inc.)
NDC Code
69097-842-15
Package Description
1000 TABLET in 1 BOTTLE (69097-842-15)
Product NDC
69097-842
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Quinapril
Non-Proprietary Name
Quinapril
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20160722
Marketing Category Name
ANDA
Application Number
ANDA078457
Manufacturer
Cipla USA Inc.
Substance Name
QUINAPRIL HYDROCHLORIDE
Strength
20
Strength Unit
mg/1
Pharmacy Classes
Angiotensin Converting Enzyme Inhibitor [EPC], Angiotensin-converting Enzyme Inhibitors [MoA]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/69097-842-15