Package 51672-4234-1

Brand: fluphenazine hydrochloride

Generic: fluphenazine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 51672-4234-1
Digits Only 5167242341
Product NDC 51672-4234
Product ID 51672-4234_2e6cbcab-4d8a-5f9a-e063-6394a90a056c
Description

100 TABLET, FILM COATED in 1 BOTTLE (51672-4234-1)

Marketing

Marketing Status
Marketed Since 2022-04-14
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": "2e6cbcab-4d8a-5f9a-e063-6394a90a056c", "openfda": {"upc": ["0351672423315", "0351672423414", "0351672423513"], "unii": ["ZOU145W1XL"], "rxcui": ["859841", "860918", "865117", "865123"], "spl_set_id": ["7036f7c6-0792-400d-a1c7-54f21b2bd481"], "manufacturer_name": ["Taro Pharmaceuticals U.S.A. Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (51672-4234-1)", "package_ndc": "51672-4234-1", "marketing_start_date": "20220414"}], "brand_name": "Fluphenazine Hydrochloride", "product_id": "51672-4234_2e6cbcab-4d8a-5f9a-e063-6394a90a056c", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "51672-4234", "generic_name": "Fluphenazine Hydrochloride", "labeler_name": "Taro Pharmaceuticals U.S.A. Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Fluphenazine Hydrochloride", "active_ingredients": [{"name": "FLUPHENAZINE HYDROCHLORIDE", "strength": "2.5 mg/1"}], "application_number": "ANDA215674", "marketing_category": "ANDA", "marketing_start_date": "20220414", "listing_expiration_date": "20261231"}