Package 50090-7226-0

Brand: fluoxetine

Generic: fluoxetine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 50090-7226-0
Digits Only 5009072260
Product NDC 50090-7226
Product ID 50090-7226_042adae3-83f7-431b-a947-3ce3680cb001
Description

90 CAPSULE in 1 BOTTLE (50090-7226-0)

Marketing

Marketing Status
Marketed Since 2024-08-20
Brand fluoxetine
Generic fluoxetine hydrochloride
Sample Package No

Linked Drug Pages (1)

Fluoxetine ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "042adae3-83f7-431b-a947-3ce3680cb001", "openfda": {"unii": ["I9W7N6B1KJ"], "rxcui": ["310385"], "spl_set_id": ["cdf3b608-e14c-474b-b80e-01ac5f701866"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 CAPSULE in 1 BOTTLE (50090-7226-0)", "package_ndc": "50090-7226-0", "marketing_start_date": "20240820"}], "brand_name": "Fluoxetine", "product_id": "50090-7226_042adae3-83f7-431b-a947-3ce3680cb001", "dosage_form": "CAPSULE", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "50090-7226", "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": "20 mg/1"}], "application_number": "ANDA204597", "marketing_category": "ANDA", "marketing_start_date": "20150316", "listing_expiration_date": "20261231"}