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"51655-793-20" National Drug Code (NDC)
Sildenafil Citrate 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-793-20)
(Northwind Health Company, LLC)
NDC Code
51655-793-20
Package Description
20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-793-20)
Product NDC
51655-793
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Sildenafil Citrate
Non-Proprietary Name
Sildenafil
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20220120
Marketing Category Name
ANDA
Application Number
ANDA204883
Manufacturer
Northwind Health Company, LLC
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/51655-793-20