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"82009-061-05" National Drug Code (NDC)
Finasteride 500 TABLET, FILM COATED in 1 BOTTLE (82009-061-05)
(QUALLENT PHARMACEUTICALS HEALTH LLC)
NDC Code
82009-061-05
Package Description
500 TABLET, FILM COATED in 1 BOTTLE (82009-061-05)
Product NDC
82009-061
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Finasteride
Non-Proprietary Name
Finasteride
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20221121
Marketing Category Name
ANDA
Application Number
ANDA078341
Manufacturer
QUALLENT PHARMACEUTICALS HEALTH LLC
Substance Name
FINASTERIDE
Strength
5
Strength Unit
mg/1
Pharmacy Classes
5-alpha Reductase Inhibitor [EPC], 5-alpha Reductase Inhibitors [MoA]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/82009-061-05