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"68151-1473-1" National Drug Code (NDC)
Moexipril Hydrochloride 1 TABLET, FILM COATED in 1 BLISTER PACK (68151-1473-1)
(Carilion Materials Management)
NDC Code
68151-1473-1
Package Description
1 TABLET, FILM COATED in 1 BLISTER PACK (68151-1473-1)
Product NDC
68151-1473
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
20030508
Marketing Category Name
ANDA
Application Number
ANDA076204
Manufacturer
Carilion Materials Management
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/68151-1473-1