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"60290-030-03" National Drug Code (NDC)
Tadalafil 30 TABLET, FILM COATED in 1 BLISTER PACK (60290-030-03)
(Umedica Laboratories USA Inc.)
NDC Code
60290-030-03
Package Description
30 TABLET, FILM COATED in 1 BLISTER PACK (60290-030-03)
Product NDC
60290-030
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Tadalafil
Non-Proprietary Name
Tadalafil
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20260215
Marketing Category Name
ANDA
Application Number
ANDA211298
Manufacturer
Umedica Laboratories USA Inc.
Substance Name
TADALAFIL
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/60290-030-03