Package 49884-336-11

Brand: fluoxetine hydrochloride

Generic: fluoxetine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 49884-336-11
Digits Only 4988433611
Product NDC 49884-336
Product ID 49884-336_71c75730-de24-4bfe-ad24-c92107cd5b74
Description

30 TABLET, COATED in 1 BOTTLE, PLASTIC (49884-336-11)

Marketing

Marketing Status
Marketed Since 2016-08-22
Brand fluoxetine hydrochloride
Generic fluoxetine hydrochloride
Sample Package No

Linked Drug Pages (1)

fluoxetine hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "71c75730-de24-4bfe-ad24-c92107cd5b74", "openfda": {"upc": ["0349884336103", "0349884335106"], "unii": ["I9W7N6B1KJ"], "rxcui": ["248642", "313990"], "spl_set_id": ["53ac797d-8792-4a8c-9708-d1de3d377e8f"], "manufacturer_name": ["Endo USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, COATED in 1 BOTTLE, PLASTIC (49884-336-01)", "package_ndc": "49884-336-01", "marketing_start_date": "20160822"}, {"sample": false, "description": "30 TABLET, COATED in 1 BOTTLE, PLASTIC (49884-336-11)", "package_ndc": "49884-336-11", "marketing_start_date": "20160822"}], "brand_name": "fluoxetine hydrochloride", "product_id": "49884-336_71c75730-de24-4bfe-ad24-c92107cd5b74", "dosage_form": "TABLET, COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "49884-336", "generic_name": "fluoxetine hydrochloride", "labeler_name": "Endo USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "fluoxetine hydrochloride", "active_ingredients": [{"name": "FLUOXETINE HYDROCHLORIDE", "strength": "20 mg/1"}], "application_number": "ANDA203836", "marketing_category": "ANDA", "marketing_start_date": "20160822", "listing_expiration_date": "20261231"}