Package 50090-6193-0

Brand: fluoxetine

Generic: fluoxetine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 50090-6193-0
Digits Only 5009061930
Product NDC 50090-6193
Description

30 CAPSULE in 1 BOTTLE (50090-6193-0)

Marketing

Marketing Status
Marketed Since 2022-10-31
Brand fluoxetine
Generic fluoxetine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "ee346fc9-8b1a-4db4-830c-b1cdf30ec29f", "openfda": {"unii": ["I9W7N6B1KJ"], "rxcui": ["310384"], "spl_set_id": ["a408c325-d2d5-4e88-85ce-96913eb58183"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BOTTLE (50090-6193-0)", "package_ndc": "50090-6193-0", "marketing_start_date": "20221031"}, {"sample": false, "description": "90 CAPSULE in 1 BOTTLE (50090-6193-2)", "package_ndc": "50090-6193-2", "marketing_start_date": "20221031"}], "brand_name": "Fluoxetine", "product_id": "50090-6193_ee346fc9-8b1a-4db4-830c-b1cdf30ec29f", "dosage_form": "CAPSULE", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "50090-6193", "generic_name": "Fluoxetine Hydrochloride", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Fluoxetine", "active_ingredients": [{"name": "FLUOXETINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA204597", "marketing_category": "ANDA", "marketing_start_date": "20150316", "listing_expiration_date": "20261231"}