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"59762-0035-2" National Drug Code (NDC)
Sildenafil Citrate 100 TABLET, FILM COATED in 1 BOTTLE (59762-0035-2)
(Greenstone LLC)
NDC Code
59762-0035-2
Package Description
100 TABLET, FILM COATED in 1 BOTTLE (59762-0035-2)
Product NDC
59762-0035
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Sildenafil Citrate
Non-Proprietary Name
Sildenafil Citrate
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20171201
Marketing Category Name
NDA AUTHORIZED GENERIC
Application Number
NDA020895
Manufacturer
Greenstone LLC
Substance Name
SILDENAFIL CITRATE
Strength
50
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/59762-0035-2