Package 69315-265-01

Brand: prochlorperazine maleate

Generic: prochlorperazine maleate
NDC Package

Package Facts

Identity

Package NDC 69315-265-01
Digits Only 6931526501
Product NDC 69315-265
Product ID 69315-265_e9585ce8-2433-4d85-ab3a-c544d7cb1532
Description

100 TABLET, FILM COATED in 1 BOTTLE (69315-265-01)

Marketing

Marketing Status
Marketed Since 2025-06-25
Brand prochlorperazine maleate
Generic prochlorperazine maleate
Sample Package No

Linked Drug Pages (1)

PROCHLORPERAZINE MALEATE ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "e9585ce8-2433-4d85-ab3a-c544d7cb1532", "openfda": {"upc": ["0369315265017", "0369315266014"], "unii": ["I1T8O1JTL6"], "rxcui": ["198365", "312635"], "spl_set_id": ["c93494ef-c510-4e46-a1b1-362624200223"], "manufacturer_name": ["Leading Pharma, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (69315-265-01)", "package_ndc": "69315-265-01", "marketing_start_date": "20250625"}], "brand_name": "PROCHLORPERAZINE MALEATE", "product_id": "69315-265_e9585ce8-2433-4d85-ab3a-c544d7cb1532", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "69315-265", "generic_name": "PROCHLORPERAZINE MALEATE", "labeler_name": "Leading Pharma, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PROCHLORPERAZINE MALEATE", "active_ingredients": [{"name": "PROCHLORPERAZINE MALEATE", "strength": "5 mg/1"}], "application_number": "ANDA218912", "marketing_category": "ANDA", "marketing_start_date": "20250625", "listing_expiration_date": "20261231"}