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"49349-302-02" National Drug Code (NDC)
Benazepril Hydrochloride 30 TABLET in 1 BLISTER PACK (49349-302-02)
(REMEDYREPACK INC.)
NDC Code
49349-302-02
Package Description
30 TABLET in 1 BLISTER PACK (49349-302-02)
Product NDC
49349-302
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Benazepril Hydrochloride
Non-Proprietary Name
Benazepril Hydrochloride
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20110616
Marketing Category Name
ANDA
Application Number
ANDA076211
Manufacturer
REMEDYREPACK INC.
Substance Name
BENAZEPRIL HYDROCHLORIDE
Strength
20
Strength Unit
mg/1
Pharmacy Classes
Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA],Decreased Blood Pressure [PE]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/49349-302-02