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"63739-072-33" National Drug Code (NDC)

Sildenafil 3 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-072-33) / 10 TABLET, FILM COATED in 1 BLISTER PACK
(McKesson Corporation dba SKY Packaging)

NDC Code63739-072-33
Package Description3 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-072-33) / 10 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC63739-072
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameSildenafil
Non-Proprietary NameSildenafil
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20220329
Marketing Category NameANDA
Application NumberANDA203623
ManufacturerMcKesson Corporation dba SKY Packaging
Substance NameSILDENAFIL CITRATE
Strength20
Strength Unitmg/1
Pharmacy ClassesPhosphodiesterase 5 Inhibitor [EPC], Phosphodiesterase 5 Inhibitors [MoA]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/63739-072-33





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