Package 68645-131-54

Brand: fluoxetine

Generic: fluoxetine
NDC Package

Package Facts

Identity

Package NDC 68645-131-54
Digits Only 6864513154
Product NDC 68645-131
Product ID 68645-131_4c222d2c-813c-5520-e063-6294a90affe6
Description

30 CAPSULE in 1 BOTTLE (68645-131-54)

Marketing

Marketing Status
Marketed Since 2011-01-25
Brand fluoxetine
Generic fluoxetine
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": "4c222d2c-813c-5520-e063-6294a90affe6", "openfda": {"upc": ["0368645130545"], "unii": ["I9W7N6B1KJ"], "rxcui": ["310384", "310385"], "spl_set_id": ["b07f9eab-44ac-4667-bd46-52d736daa5d6"], "manufacturer_name": ["Legacy Pharmaceutical Packaging, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BOTTLE (68645-131-54)", "package_ndc": "68645-131-54", "marketing_start_date": "20110125"}], "brand_name": "Fluoxetine", "product_id": "68645-131_4c222d2c-813c-5520-e063-6294a90affe6", "dosage_form": "CAPSULE", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "68645-131", "generic_name": "Fluoxetine", "labeler_name": "Legacy Pharmaceutical Packaging, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Fluoxetine", "active_ingredients": [{"name": "FLUOXETINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA076001", "marketing_category": "ANDA", "marketing_start_date": "20110125", "listing_expiration_date": "20271231"}