Package 0121-0654-02
Brand: fluphenazine hydrochloride
Generic: fluphenazine hydrochloridePackage Facts
Identity
Package NDC
0121-0654-02
Digits Only
0121065402
Product NDC
0121-0654
Description
60 mL in 1 BOTTLE (0121-0654-02)
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": "be2cdaa4-74b5-4256-90c0-e1410973b3f5", "openfda": {"upc": ["0301210654022"], "unii": ["ZOU145W1XL"], "rxcui": ["859835"], "spl_set_id": ["f0a89d5d-01db-47f3-a873-33ab49c6e4f8"], "manufacturer_name": ["PAI Holdings, LLC dba PAI Pharma"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 mL in 1 BOTTLE (0121-0654-02)", "package_ndc": "0121-0654-02", "marketing_start_date": "20100831"}, {"sample": false, "description": "473 mL in 1 BOTTLE (0121-0654-16)", "package_ndc": "0121-0654-16", "marketing_start_date": "20100831"}], "brand_name": "Fluphenazine Hydrochloride", "product_id": "0121-0654_be2cdaa4-74b5-4256-90c0-e1410973b3f5", "dosage_form": "ELIXIR", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "0121-0654", "generic_name": "Fluphenazine Hydrochloride", "labeler_name": "PAI Holdings, LLC dba PAI Pharma", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Fluphenazine Hydrochloride", "active_ingredients": [{"name": "FLUPHENAZINE HYDROCHLORIDE", "strength": ".5 mg/mL"}], "application_number": "ANDA040146", "marketing_category": "ANDA", "marketing_start_date": "20100831", "listing_expiration_date": "20261231"}