Package 24979-139-01

Brand: fluphenazine hydrochloride

Generic: fluphenazine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 24979-139-01
Digits Only 2497913901
Product NDC 24979-139
Product ID 24979-139_e2589baf-4d61-4d50-a578-41c51fbb6deb
Description

100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (24979-139-01)

Marketing

Marketing Status
Marketed Since 2022-08-01
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": "e2589baf-4d61-4d50-a578-41c51fbb6deb", "openfda": {"upc": ["0324979139012", "0324979138015", "0324979137018", "0324979136011"], "unii": ["ZOU145W1XL"], "rxcui": ["859841", "860918", "865117", "865123"], "spl_set_id": ["d0a090fa-f7c9-4f6d-a9a3-9838870c7049"], "manufacturer_name": ["Upsher-Smith Laboratories, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (24979-139-01)", "package_ndc": "24979-139-01", "marketing_start_date": "20220801"}], "brand_name": "Fluphenazine Hydrochloride", "product_id": "24979-139_e2589baf-4d61-4d50-a578-41c51fbb6deb", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "24979-139", "generic_name": "Fluphenazine Hydrochloride", "labeler_name": "Upsher-Smith Laboratories, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Fluphenazine Hydrochloride", "active_ingredients": [{"name": "FLUPHENAZINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA215848", "marketing_category": "ANDA", "marketing_start_date": "20220801", "listing_expiration_date": "20261231"}