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"70518-4221-0" National Drug Code (NDC)
Sildenafil Citrate 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4221-0)
(REMEDYREPACK INC.)
NDC Code
70518-4221-0
Package Description
20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4221-0)
Product NDC
70518-4221
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Sildenafil Citrate
Non-Proprietary Name
Sildenafil
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20241023
Marketing Category Name
ANDA
Application Number
ANDA091448
Manufacturer
REMEDYREPACK 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/70518-4221-0