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"68382-899-10" National Drug Code (NDC)
Tadalafil 1000 TABLET, FILM COATED in 1 BOTTLE (68382-899-10)
(Zydus Pharmaceuticals USA Inc.)
NDC Code
68382-899-10
Package Description
1000 TABLET, FILM COATED in 1 BOTTLE (68382-899-10)
Product NDC
68382-899
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Tadalafil
Non-Proprietary Name
Tadalafil
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20190327
Marketing Category Name
ANDA
Application Number
ANDA206693
Manufacturer
Zydus Pharmaceuticals 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/68382-899-10