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"49884-734-10" National Drug Code (NDC)
Fluoxetine Hydrochloride 1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (49884-734-10)
(Par Pharmaceutical, Inc)
NDC Code
49884-734-10
Package Description
1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (49884-734-10)
Product NDC
49884-734
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Fluoxetine Hydrochloride
Non-Proprietary Name
Fluoxetine Hydrochloride
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20010802
End Marketing Date
20161130
Marketing Category Name
ANDA
Application Number
ANDA075755
Manufacturer
Par Pharmaceutical, Inc
Substance Name
FLUOXETINE HYDROCHLORIDE
Strength
10
Strength Unit
mg/1
Pharmacy Classes
Serotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/49884-734-10