NDC 42291-652

Olanzapine and Fluoxetine

Olanzapine And Fluoxetine

Olanzapine and Fluoxetine is a Oral Capsule in the Human Prescription Drug category. It is labeled and distributed by Avkare, Inc.. The primary component is Olanzapine; Fluoxetine Hydrochloride.

Product ID42291-652_7cad8747-2c88-a06d-e053-2a91aa0a7722
NDC42291-652
Product TypeHuman Prescription Drug
Proprietary NameOlanzapine and Fluoxetine
Generic NameOlanzapine And Fluoxetine
Dosage FormCapsule
Route of AdministrationORAL
Marketing Start Date2014-01-21
Marketing CategoryANDA / ANDA
Application NumberANDA202074
Labeler NameAvKARE, Inc.
Substance NameOLANZAPINE; FLUOXETINE HYDROCHLORIDE
Active Ingredient Strength3 mg/1; mg/1
Pharm ClassesAtypical Antipsychotic [EPC],Serotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 42291-652-30

30 CAPSULE in 1 BOTTLE (42291-652-30)
Marketing Start Date2014-01-21
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 42291-652-30 [42291065230]

Olanzapine and Fluoxetine CAPSULE
Marketing CategoryANDA
Application NumberANDA202074
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2014-01-21

Drug Details

Active Ingredients

IngredientStrength
OLANZAPINE3 mg/1

OpenFDA Data

SPL SET ID:f5f78ed2-4640-8528-c51c-d7bffa045d48
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 403969
  • 721787
  • 403972
  • 403971
  • 403970
  • UPC Code
  • 0342291655300
  • 0342291656307
  • 0342291654303
  • 0342291653306
  • Pharmacological Class

    • Atypical Antipsychotic [EPC]
    • Serotonin Reuptake Inhibitor [EPC]
    • Serotonin Uptake Inhibitors [MoA]
    • Atypical Antipsychotic [EPC]
    • Serotonin Reuptake Inhibitor [EPC]
    • Serotonin Uptake Inhibitors [MoA]

    NDC Crossover Matching brand name "Olanzapine and Fluoxetine" or generic name "Olanzapine And Fluoxetine"

    NDCBrand NameGeneric Name
    0093-5503Olanzapine and FluoxetineOlanzapine and Fluoxetine
    0093-5504Olanzapine and FluoxetineOlanzapine and Fluoxetine
    0093-5505Olanzapine and FluoxetineOlanzapine and Fluoxetine
    0093-5506Olanzapine and FluoxetineOlanzapine and Fluoxetine
    0093-5507Olanzapine and FluoxetineOlanzapine and Fluoxetine
    0781-2191Olanzapine and FluoxetineOlanzapine and Fluoxetine
    0781-2192Olanzapine and FluoxetineOlanzapine and Fluoxetine
    0781-2193Olanzapine and FluoxetineOlanzapine and Fluoxetine
    0781-2194Olanzapine and FluoxetineOlanzapine and Fluoxetine
    0781-2195Olanzapine and FluoxetineOlanzapine and Fluoxetine
    42291-655Olanzapine and FluoxetineOlanzapine and Fluoxetine
    42291-652Olanzapine and FluoxetineOlanzapine and Fluoxetine
    42291-654Olanzapine and FluoxetineOlanzapine and Fluoxetine
    42291-656Olanzapine and FluoxetineOlanzapine and Fluoxetine
    42291-653Olanzapine and FluoxetineOlanzapine and Fluoxetine
    49884-253Olanzapine and FluoxetineOlanzapine and Fluoxetine
    49884-251Olanzapine and FluoxetineOlanzapine and Fluoxetine
    49884-252Olanzapine and FluoxetineOlanzapine and Fluoxetine
    49884-277Olanzapine and FluoxetineOlanzapine and Fluoxetine
    49884-250Olanzapine and FluoxetineOlanzapine and Fluoxetine

    © 2024 FDA.report
    This site is not affiliated with or endorsed by the FDA.