Package 0527-1791-01

Brand: fluphenazine hydrochloride

Generic: fluphenazine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0527-1791-01
Digits Only 0527179101
Product NDC 0527-1791
Product ID 0527-1791_59cf1ea7-b827-4780-bf94-cd3446d6dcc3
Description

100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0527-1791-01)

Marketing

Marketing Status
Marketed Since 1988-08-25
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": "59cf1ea7-b827-4780-bf94-cd3446d6dcc3", "openfda": {"upc": ["0305271791016", "0305271790019", "0305271789013"], "unii": ["ZOU145W1XL"], "rxcui": ["859841", "860918", "865117", "865123"], "spl_set_id": ["6cd6ba35-3481-48c1-87db-dc74ce9d7d75"], "manufacturer_name": ["Lannett Company, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0527-1791-01)", "package_ndc": "0527-1791-01", "marketing_start_date": "19880825"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0527-1791-05)", "package_ndc": "0527-1791-05", "marketing_start_date": "19880825"}], "brand_name": "Fluphenazine Hydrochloride", "product_id": "0527-1791_59cf1ea7-b827-4780-bf94-cd3446d6dcc3", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "0527-1791", "generic_name": "Fluphenazine Hydrochloride", "labeler_name": "Lannett Company, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Fluphenazine Hydrochloride", "active_ingredients": [{"name": "FLUPHENAZINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA089743", "marketing_category": "ANDA", "marketing_start_date": "19880825", "listing_expiration_date": "20261231"}