Package 62332-790-31

Brand: fluphenazine hydrochloride

Generic: fluphenazine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 62332-790-31
Digits Only 6233279031
Product NDC 62332-790
Product ID 62332-790_f7ef2923-6d2a-4b1f-ad9c-c8127391b9f4
Description

100 TABLET, FILM COATED in 1 BOTTLE (62332-790-31)

Marketing

Marketing Status
Marketed Since 2024-07-25
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": "f7ef2923-6d2a-4b1f-ad9c-c8127391b9f4", "openfda": {"upc": ["0362332790319", "0362332788316", "0362332789313", "0362332791316"], "unii": ["ZOU145W1XL"], "rxcui": ["859841", "860918", "865117", "865123"], "spl_set_id": ["1991be2c-9629-4c3e-93f0-e40bcffc82b0"], "manufacturer_name": ["Alembic Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (62332-790-31)", "package_ndc": "62332-790-31", "marketing_start_date": "20240725"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (62332-790-71)", "package_ndc": "62332-790-71", "marketing_start_date": "20240725"}], "brand_name": "Fluphenazine Hydrochloride", "product_id": "62332-790_f7ef2923-6d2a-4b1f-ad9c-c8127391b9f4", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "62332-790", "generic_name": "Fluphenazine Hydrochloride", "labeler_name": "Alembic Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Fluphenazine Hydrochloride", "active_ingredients": [{"name": "FLUPHENAZINE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA218173", "marketing_category": "ANDA", "marketing_start_date": "20240725", "listing_expiration_date": "20261231"}