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"60687-788-21" National Drug Code (NDC)
Sildenafil 30 BLISTER PACK in 1 CARTON (60687-788-21) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-788-11)
(American Health Packaging)
NDC Code
60687-788-21
Package Description
30 BLISTER PACK in 1 CARTON (60687-788-21) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-788-11)
Product NDC
60687-788
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Sildenafil
Non-Proprietary Name
Sildenafil
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20231113
Marketing Category Name
ANDA
Application Number
ANDA203814
Manufacturer
American Health Packaging
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/60687-788-21