Package 69367-235-10

Brand: fluoxetine

Generic: fluoxetine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 69367-235-10
Digits Only 6936723510
Product NDC 69367-235
Product ID 69367-235_2c8c16fd-61b1-4d89-bbc5-66d4d7c0a770
Description

1000 CAPSULE in 1 BOTTLE (69367-235-10)

Marketing

Marketing Status
Discontinued 2026-08-01
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": "2c8c16fd-61b1-4d89-bbc5-66d4d7c0a770", "openfda": {"unii": ["I9W7N6B1KJ"], "rxcui": ["310384", "310385", "313989"], "spl_set_id": ["8c4b2119-8cec-4b4b-9a52-ae763fd9b252"], "manufacturer_name": ["Westminster Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (69367-235-01)", "package_ndc": "69367-235-01", "marketing_end_date": "20260801", "marketing_start_date": "20190925"}, {"sample": false, "description": "1000 CAPSULE in 1 BOTTLE (69367-235-10)", "package_ndc": "69367-235-10", "marketing_end_date": "20260801", "marketing_start_date": "20190925"}], "brand_name": "Fluoxetine", "product_id": "69367-235_2c8c16fd-61b1-4d89-bbc5-66d4d7c0a770", "dosage_form": "CAPSULE", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "69367-235", "generic_name": "Fluoxetine Hydrochloride", "labeler_name": "Westminster Pharmaceuticals, LLC", "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_end_date": "20260801", "marketing_start_date": "20190925"}