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"71205-721-04" National Drug Code (NDC)
Sildenafil Citrate 4 TABLET in 1 BOTTLE (71205-721-04)
(Proficient Rx LP)
NDC Code
71205-721-04
Package Description
4 TABLET in 1 BOTTLE (71205-721-04)
Product NDC
71205-721
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Sildenafil Citrate
Non-Proprietary Name
Sildenafil Citrate
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20200904
Marketing Category Name
ANDA
Application Number
ANDA209302
Manufacturer
Proficient Rx LP
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/71205-721-04