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"60290-003-03" National Drug Code (NDC)
Sildenafil Citrate 1000 TABLET, FILM COATED in 1 BOTTLE (60290-003-03)
(Umedica Laboratories USA Inc.)
NDC Code
60290-003-03
Package Description
1000 TABLET, FILM COATED in 1 BOTTLE (60290-003-03)
Product NDC
60290-003
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
20260215
Marketing Category Name
ANDA
Application Number
ANDA209302
Manufacturer
Umedica Laboratories USA Inc.
Substance Name
SILDENAFIL CITRATE
Strength
100
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/60290-003-03