NDC 49884-734

NDC 49884-734

NDC 49884-734 is a in the category. It is labeled and distributed by .

Proprietary NameNDC 49884-734
Marketing Category/

Packaging

NDC SPL Data Element Entries

NDC 49884-734-10 [49884073410]

Fluoxetine Hydrochloride TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA075755
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2001-08-02
Marketing End Date2016-11-30

NDC 49884-734-01 [49884073401]

Fluoxetine Hydrochloride TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA075755
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2001-08-02
Marketing End Date2016-11-30

NDC 49884-734-11 [49884073411]

Fluoxetine Hydrochloride TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA075755
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2001-08-02
Marketing End Date2016-11-30

NDC 49884-734-82 [49884073482]

Fluoxetine Hydrochloride TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA075755
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2010-01-13
Marketing End Date2011-07-31

Drug Details

Medicade Reported Pricing

49884073411 FLUOXETINE HCL 10 MG TABLET

Pricing Unit: EA | Drug Type:

49884073410 FLUOXETINE HCL 10 MG TABLET

Pricing Unit: EA | Drug Type:

49884073401 FLUOXETINE HCL 10 MG TABLET

Pricing Unit: EA | Drug Type:
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