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"0574-0112-15" National Drug Code (NDC)
Moexipril Hydrochloride 100 TABLET, COATED in 1 BOTTLE, PLASTIC (0574-0112-15)
(Paddock Laboratories, Inc.)
NDC Code
0574-0112-15
Package Description
100 TABLET, COATED in 1 BOTTLE, PLASTIC (0574-0112-15)
Product NDC
0574-0112
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Moexipril Hydrochloride
Non-Proprietary Name
Moexipril Hydrochloride
Dosage Form
TABLET, COATED
Usage
ORAL
Start Marketing Date
20061130
Marketing Category Name
ANDA
Application Number
ANDA077536
Manufacturer
Paddock Laboratories, Inc.
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/0574-0112-15