Package 62135-418-90

Brand: fluphenazine hydrochloride

Generic: fluphenazine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 62135-418-90
Digits Only 6213541890
Product NDC 62135-418
Description

90 TABLET, FILM COATED in 1 BOTTLE (62135-418-90)

Marketing

Marketing Status
Marketed Since 2022-10-20
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": "458c6457-ed15-15f4-e063-6294a90acc6d", "openfda": {"upc": ["0362135416904", "0362135418908", "0362135419905", "0362135415907"], "unii": ["ZOU145W1XL"], "rxcui": ["859841", "860918", "865117", "865123"], "spl_set_id": ["325af2a4-2280-4236-8cf8-44f5700ba73f"], "manufacturer_name": ["Chartwell RX, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (62135-418-90)", "package_ndc": "62135-418-90", "marketing_start_date": "20221020"}], "brand_name": "fluphenazine hydrochloride", "product_id": "62135-418_458c6457-ed15-15f4-e063-6294a90acc6d", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "62135-418", "generic_name": "fluphenazine hydrochloride", "labeler_name": "Chartwell RX, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "fluphenazine hydrochloride", "active_ingredients": [{"name": "FLUPHENAZINE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA215141", "marketing_category": "ANDA", "marketing_start_date": "20220101", "listing_expiration_date": "20261231"}