Package 62135-416-90
Brand: fluphenazine hydrochloride
Generic: fluphenazine hydrochloridePackage Facts
Identity
Package NDC
62135-416-90
Digits Only
6213541690
Product NDC
62135-416
Description
90 TABLET, FILM COATED in 1 BOTTLE (62135-416-90)
Marketing
Marketing Status
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 (62135-416-90)", "package_ndc": "62135-416-90", "marketing_start_date": "20221020"}], "brand_name": "fluphenazine hydrochloride", "product_id": "62135-416_458c6457-ed15-15f4-e063-6294a90acc6d", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "62135-416", "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": "2.5 mg/1"}], "application_number": "ANDA215141", "marketing_category": "ANDA", "marketing_start_date": "20220101", "listing_expiration_date": "20261231"}