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"53002-1719-3" National Drug Code (NDC)
Sildenafil 30 TABLET, FILM COATED in 1 BOTTLE (53002-1719-3)
(RPK Pharmaceuticals, Inc.)
NDC Code
53002-1719-3
Package Description
30 TABLET, FILM COATED in 1 BOTTLE (53002-1719-3)
Product NDC
53002-1719
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Sildenafil
Non-Proprietary Name
Sildenafil
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20130531
Marketing Category Name
ANDA
Application Number
ANDA078380
Manufacturer
RPK Pharmaceuticals, Inc.
Substance Name
SILDENAFIL CITRATE
Strength
20
Strength Unit
mg/1
Pharmacy Classes
Phosphodiesterase 5 Inhibitor [EPC], Phosphodiesterase 5 Inhibitors [MoA]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/53002-1719-3