Package 55154-2638-0

Brand: fluoxetine

Generic: fluoxetine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 55154-2638-0
Digits Only 5515426380
Product NDC 55154-2638
Product ID 55154-2638_97385230-4710-47cf-9617-fc0f2fef78b3
Description

10 BLISTER PACK in 1 BAG (55154-2638-0) / 1 CAPSULE in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2024-12-04
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": "97385230-4710-47cf-9617-fc0f2fef78b3", "openfda": {"upc": ["0055154263801"], "unii": ["I9W7N6B1KJ"], "rxcui": ["310385"], "spl_set_id": ["06394c4b-99f4-4257-bf29-53c170c5a061"], "manufacturer_name": ["Cardinal Health 107, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "10 BLISTER PACK in 1 BAG (55154-2638-0)  / 1 CAPSULE in 1 BLISTER PACK", "package_ndc": "55154-2638-0", "marketing_start_date": "20241204"}], "brand_name": "Fluoxetine", "product_id": "55154-2638_97385230-4710-47cf-9617-fc0f2fef78b3", "dosage_form": "CAPSULE", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "55154-2638", "generic_name": "Fluoxetine Hydrochloride", "labeler_name": "Cardinal Health 107, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Fluoxetine", "active_ingredients": [{"name": "FLUOXETINE HYDROCHLORIDE", "strength": "20 mg/1"}], "application_number": "ANDA078619", "marketing_category": "ANDA", "marketing_start_date": "20241204", "listing_expiration_date": "20261231"}