Package 17224-174-21

Brand: fluoxetine

Generic: fluoxetine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 17224-174-21
Digits Only 1722417421
Product NDC 17224-174
Product ID 17224-174_1661c5e0-7a8b-431e-e063-6294a90a434b
Description

21 CAPSULE in 1 BOTTLE, PLASTIC (17224-174-21)

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": "1661c5e0-7a8b-431e-e063-6294a90a434b", "openfda": {"unii": ["I9W7N6B1KJ"], "rxcui": ["310385"], "spl_set_id": ["4915e22f-cecb-4261-8389-9bb417a20e82"], "manufacturer_name": ["Calvin Scott & Co., Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "21 CAPSULE in 1 BOTTLE, PLASTIC (17224-174-21)", "package_ndc": "17224-174-21", "marketing_start_date": "20150316"}], "brand_name": "Fluoxetine", "product_id": "17224-174_1661c5e0-7a8b-431e-e063-6294a90a434b", "dosage_form": "CAPSULE", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "17224-174", "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": "20 mg/1"}], "application_number": "ANDA204597", "marketing_category": "ANDA", "marketing_start_date": "20150316", "listing_expiration_date": "20261231"}