Package 72205-115-05

Brand: fluphenazine hydrochloride

Generic: fluphenazine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72205-115-05
Digits Only 7220511505
Product NDC 72205-115
Description

500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72205-115-05)

Marketing

Marketing Status
Marketed Since 2023-09-14
Brand fluphenazine hydrochloride
Generic fluphenazine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "f99e9ea5-3c4a-4a94-9ca9-709f65b8fd82", "openfda": {"upc": ["0372205115910", "0372205114913", "0372205112919", "0372205113916", "0372205114050", "0372205112056", "0372205113053"], "unii": ["ZOU145W1XL"], "rxcui": ["859841", "860918", "865117", "865123"], "spl_set_id": ["83ce71b9-28eb-4074-b1e7-192ed254c529"], "manufacturer_name": ["Novadoz Pharmaceuticals LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72205-115-05)", "package_ndc": "72205-115-05", "marketing_start_date": "20230914"}, {"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72205-115-91)", "package_ndc": "72205-115-91", "marketing_start_date": "20230914"}], "brand_name": "Fluphenazine Hydrochloride", "product_id": "72205-115_f99e9ea5-3c4a-4a94-9ca9-709f65b8fd82", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "72205-115", "generic_name": "Fluphenazine Hydrochloride", "labeler_name": "Novadoz Pharmaceuticals LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Fluphenazine Hydrochloride", "active_ingredients": [{"name": "FLUPHENAZINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA217189", "marketing_category": "ANDA", "marketing_start_date": "20230911", "listing_expiration_date": "20261231"}