"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 Code60687-788-21
Package Description30 BLISTER PACK in 1 CARTON (60687-788-21) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-788-11)
Product NDC60687-788
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameSildenafil
Non-Proprietary NameSildenafil
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20231113
Marketing Category NameANDA
Application NumberANDA203814
ManufacturerAmerican Health Packaging
Substance NameSILDENAFIL CITRATE
Strength20
Strength Unitmg/1
Pharmacy ClassesPhosphodiesterase 5 Inhibitor [EPC], Phosphodiesterase 5 Inhibitors [MoA]

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