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"60290-029-03" National Drug Code (NDC)

Tadalafil 30 TABLET, FILM COATED in 1 BLISTER PACK (60290-029-03)
(Umedica Laboratories USA Inc.)

NDC Code60290-029-03
Package Description30 TABLET, FILM COATED in 1 BLISTER PACK (60290-029-03)
Product NDC60290-029
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameTadalafil
Non-Proprietary NameTadalafil
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20260215
Marketing Category NameANDA
Application NumberANDA211298
ManufacturerUmedica Laboratories USA Inc.
Substance NameTADALAFIL
Strength10
Strength Unitmg/1
Pharmacy ClassesPhosphodiesterase 5 Inhibitor [EPC], Phosphodiesterase 5 Inhibitors [MoA]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/60290-029-03





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