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"62135-969-90" National Drug Code (NDC)
Moexipril Hydrochloride 90 TABLET, FILM COATED in 1 BOTTLE (62135-969-90)
(Chartwell RX, LLC)
NDC Code
62135-969-90
Package Description
90 TABLET, FILM COATED in 1 BOTTLE (62135-969-90)
Product NDC
62135-969
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Moexipril Hydrochloride
Non-Proprietary Name
Moexipril Hydrochloride
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20061130
Marketing Category Name
ANDA
Application Number
ANDA077536
Manufacturer
Chartwell RX, LLC
Substance Name
MOEXIPRIL HYDROCHLORIDE
Strength
15
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/62135-969-90