Package 50268-366-15

Brand: fluphenazine hydrochloride

Generic: fluphenazine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 50268-366-15
Digits Only 5026836615
Product NDC 50268-366
Product ID 50268-366_2b4993c9-b528-9f47-e063-6394a90a7a4d
Description

50 BLISTER PACK in 1 BOX (50268-366-15) / 1 TABLET, FILM COATED in 1 BLISTER PACK (50268-366-11)

Marketing

Marketing Status
Marketed Since 2022-07-06
Brand fluphenazine hydrochloride
Generic fluphenazine hydrochloride
Sample Package No

Linked Drug Pages (1)

Fluphenazine Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "2b4993c9-b528-9f47-e063-6394a90a7a4d", "openfda": {"unii": ["ZOU145W1XL"], "rxcui": ["860918", "865117", "865123"], "spl_set_id": ["e3277017-1d58-7105-e053-2995a90a9255"], "manufacturer_name": ["AvPAK"]}, "finished": true, "packaging": [{"sample": false, "description": "50 BLISTER PACK in 1 BOX (50268-366-15)  / 1 TABLET, FILM COATED in 1 BLISTER PACK (50268-366-11)", "package_ndc": "50268-366-15", "marketing_start_date": "20220706"}], "brand_name": "Fluphenazine Hydrochloride", "product_id": "50268-366_2b4993c9-b528-9f47-e063-6394a90a7a4d", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "50268-366", "generic_name": "Fluphenazine Hydrochloride", "labeler_name": "AvPAK", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Fluphenazine Hydrochloride", "active_ingredients": [{"name": "FLUPHENAZINE HYDROCHLORIDE", "strength": "1 mg/1"}], "application_number": "ANDA214534", "marketing_category": "ANDA", "marketing_start_date": "20220706", "listing_expiration_date": "20261231"}