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"48792-7889-1" National Drug Code (NDC)
Tadalafil 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (48792-7889-1)
(Sunshine Lake Pharma Co., Ltd.)
NDC Code
48792-7889-1
Package Description
30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (48792-7889-1)
Product NDC
48792-7889
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
ANDA211335
Manufacturer
Sunshine Lake Pharma Co., Ltd.
Substance Name
TADALAFIL
Strength
10
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/48792-7889-1