Package 17224-171-30

Brand: fluoxetine

Generic: fluoxetine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 17224-171-30
Digits Only 1722417130
Product NDC 17224-171
Description

30 CAPSULE in 1 BOTTLE (17224-171-30)

Marketing

Marketing Status
Marketed Since 2015-03-16
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": "f709b80f-6425-790e-e053-6394a90a17fc", "openfda": {"unii": ["I9W7N6B1KJ"], "rxcui": ["310384"], "spl_set_id": ["3453755b-3ed6-47a3-b4c7-c64758e7784c"], "manufacturer_name": ["Calvin Scott & Co., Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "21 CAPSULE in 1 BOTTLE (17224-171-21)", "package_ndc": "17224-171-21", "marketing_start_date": "20150316"}, {"sample": false, "description": "30 CAPSULE in 1 BOTTLE (17224-171-30)", "package_ndc": "17224-171-30", "marketing_start_date": "20150316"}], "brand_name": "Fluoxetine", "product_id": "17224-171_f709b80f-6425-790e-e053-6394a90a17fc", "dosage_form": "CAPSULE", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "17224-171", "generic_name": "FLUOXETINE HYDROCHLORIDE", "labeler_name": "Calvin Scott & Co., Inc.", "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"}