Package 72162-2221-5

Brand: fluoxetine

Generic: fluoxetine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72162-2221-5
Digits Only 7216222215
Product NDC 72162-2221
Product ID 72162-2221_77d5c10a-0cfc-4b89-942c-0fb5c67ae409
Description

500 CAPSULE in 1 BOTTLE (72162-2221-5)

Marketing

Marketing Status
Marketed Since 2015-03-16
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": "77d5c10a-0cfc-4b89-942c-0fb5c67ae409", "openfda": {"unii": ["I9W7N6B1KJ"], "rxcui": ["313989"], "spl_set_id": ["77d5c10a-0cfc-4b89-942c-0fb5c67ae409"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "500 CAPSULE in 1 BOTTLE (72162-2221-5)", "package_ndc": "72162-2221-5", "marketing_start_date": "20150316"}], "brand_name": "Fluoxetine", "product_id": "72162-2221_77d5c10a-0cfc-4b89-942c-0fb5c67ae409", "dosage_form": "CAPSULE", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "72162-2221", "generic_name": "Fluoxetine Hydrochloride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Fluoxetine", "active_ingredients": [{"name": "FLUOXETINE HYDROCHLORIDE", "strength": "40 mg/1"}], "application_number": "ANDA204597", "marketing_category": "ANDA", "marketing_start_date": "20150316", "listing_expiration_date": "20261231"}