Olanzapine And Fluoxetine 00093-5507

Product NDC

00093-5507

Manufacturer: Teva Pharmaceuticals Usa, Inc.
Dosage Form: Capsule
Route: Oral
Product Type: Human Prescription Drug
Marketing Start: June 19, 2012
Listing Expires: December 31, 2027
Application: ANDA077528

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Active Ingredients

Ingredient	Strength
Fluoxetine Hydrochloride	50 mg/1
Olanzapine	12 mg/1

Drug Class

Atypical Antipsychotic [EPC]Atypical Antipsychotic [EPC]Serotonin Reuptake Inhibitor [EPC]

Packaging Options(1)

00093-5507-56

30 CAPSULE in 1 BOTTLE (0093-5507-56)

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