Package 69238-1681-1

Brand: fluphenazine hydrochloride

Generic: fluphenazine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 69238-1681-1
Digits Only 6923816811
Product NDC 69238-1681
Product ID 69238-1681_47a90e7b-4fe1-47a7-a427-de52037fb30b
Description

100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (69238-1681-1)

Marketing

Marketing Status
Marketed Since 2020-07-11
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": "47a90e7b-4fe1-47a7-a427-de52037fb30b", "openfda": {"unii": ["ZOU145W1XL"], "rxcui": ["859841", "860918", "865117", "865123"], "spl_set_id": ["5b443b30-5682-4cf3-9ed0-716efddbc865"], "manufacturer_name": ["Amneal Pharmaceuticals NY LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (69238-1681-1)", "package_ndc": "69238-1681-1", "marketing_start_date": "20200711"}], "brand_name": "fluphenazine hydrochloride", "product_id": "69238-1681_47a90e7b-4fe1-47a7-a427-de52037fb30b", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "69238-1681", "generic_name": "fluphenazine hydrochloride", "labeler_name": "Amneal Pharmaceuticals NY LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "fluphenazine hydrochloride", "active_ingredients": [{"name": "FLUPHENAZINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA213647", "marketing_category": "ANDA", "marketing_start_date": "20200711", "listing_expiration_date": "20261231"}