Package 60687-761-01

Brand: fluphenazine hydrochloride

Generic: fluphenazine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 60687-761-01
Digits Only 6068776101
Product NDC 60687-761
Product ID 60687-761_365e2405-914b-bc98-e063-6394a90adf9a
Description

100 BLISTER PACK in 1 CARTON (60687-761-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-761-11)

Marketing

Marketing Status
Marketed Since 2023-11-09
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": "365e2405-914b-bc98-e063-6394a90adf9a", "openfda": {"unii": ["ZOU145W1XL"], "rxcui": ["859841", "860918"], "spl_set_id": ["b6eadd59-a7d0-400e-ba1d-795b9243f77d"], "manufacturer_name": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 CARTON (60687-761-01)  / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-761-11)", "package_ndc": "60687-761-01", "marketing_start_date": "20231109"}], "brand_name": "Fluphenazine Hydrochloride", "product_id": "60687-761_365e2405-914b-bc98-e063-6394a90adf9a", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "60687-761", "generic_name": "Fluphenazine Hydrochloride", "labeler_name": "American Health Packaging", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Fluphenazine Hydrochloride", "active_ingredients": [{"name": "FLUPHENAZINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA214534", "marketing_category": "ANDA", "marketing_start_date": "20231109", "listing_expiration_date": "20261231"}