Package 27241-255-01
Brand: fluphenazine hydrochloride
Generic: fluphenazine hydrochloridePackage Facts
Identity
Package NDC
27241-255-01
Digits Only
2724125501
Product NDC
27241-255
Description
100 TABLET in 1 BOTTLE (27241-255-01)
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": "0069bda4-a743-4edd-a15f-a53cba1a2bff", "openfda": {"upc": ["0327241255014", "0327241252013", "0327241253010", "0327241254017"], "unii": ["ZOU145W1XL"], "rxcui": ["859841", "860918", "865117", "865123"], "spl_set_id": ["47695e20-9c0b-4a6b-ab1a-1dfaa75e96d8"], "manufacturer_name": ["Ajanta Pharma USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (27241-255-01)", "package_ndc": "27241-255-01", "marketing_start_date": "20230105"}], "brand_name": "Fluphenazine hydrochloride", "product_id": "27241-255_0069bda4-a743-4edd-a15f-a53cba1a2bff", "dosage_form": "TABLET", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "27241-255", "generic_name": "Fluphenazine hydrochloride", "labeler_name": "Ajanta Pharma USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Fluphenazine hydrochloride", "active_ingredients": [{"name": "FLUPHENAZINE HYDROCHLORIDE", "strength": "1 mg/1"}], "application_number": "ANDA217410", "marketing_category": "ANDA", "marketing_start_date": "20230105", "listing_expiration_date": "20271231"}