Package 49884-468-11

Brand: fluoxetine

Generic: fluoxetine
NDC Package

Package Facts

Identity

Package NDC 49884-468-11
Digits Only 4988446811
Product NDC 49884-468
Product ID 49884-468_ea0f9b50-185b-4a12-824e-3a7628aa0906
Description

30 TABLET, FILM COATED in 1 BOTTLE (49884-468-11)

Marketing

Marketing Status
Marketed Since 2017-11-16
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": "ea0f9b50-185b-4a12-824e-3a7628aa0906", "openfda": {"unii": ["I9W7N6B1KJ"], "rxcui": ["1190110"], "spl_set_id": ["6fff3732-efc3-4cbd-a8fa-cde3181f03e6"], "manufacturer_name": ["Endo USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (49884-468-11)", "package_ndc": "49884-468-11", "marketing_start_date": "20171116"}], "brand_name": "Fluoxetine", "product_id": "49884-468_ea0f9b50-185b-4a12-824e-3a7628aa0906", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "49884-468", "generic_name": "Fluoxetine", "labeler_name": "Endo USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Fluoxetine", "active_ingredients": [{"name": "FLUOXETINE HYDROCHLORIDE", "strength": "60 mg/1"}], "application_number": "ANDA209419", "marketing_category": "ANDA", "marketing_start_date": "20171116", "listing_expiration_date": "20261231"}