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"61919-887-30" National Drug Code (NDC)
Tadalafil 30 TABLET, FILM COATED in 1 BOTTLE (61919-887-30)
(Direct_Rx)
NDC Code
61919-887-30
Package Description
30 TABLET, FILM COATED in 1 BOTTLE (61919-887-30)
Product NDC
61919-887
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Tadalafil
Non-Proprietary Name
Tadalafil
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20190612
Marketing Category Name
ANDA
Application Number
ANDA209908
Manufacturer
Direct_Rx
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/61919-887-30