Package 69452-309-32

Brand: prochlorperazine maleate

Generic: prochlorperazine maleate
NDC Package

Package Facts

Identity

Package NDC 69452-309-32
Digits Only 6945230932
Product NDC 69452-309
Product ID 69452-309_2f9f880c-a70d-317b-e063-6294a90a2280
Description

1000 TABLET, FILM COATED in 1 BOTTLE (69452-309-32)

Marketing

Marketing Status
Marketed Since 2023-09-13
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": "2f9f880c-a70d-317b-e063-6294a90a2280", "openfda": {"upc": ["0369452310205", "0369452309209"], "unii": ["I1T8O1JTL6"], "rxcui": ["198365", "312635"], "spl_set_id": ["052d351a-978b-6fc3-e063-6294a90aef55"], "manufacturer_name": ["Bionpharma Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (69452-309-20)", "package_ndc": "69452-309-20", "marketing_start_date": "20230913"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (69452-309-32)", "package_ndc": "69452-309-32", "marketing_start_date": "20230913"}], "brand_name": "PROCHLORPERAZINE MALEATE", "product_id": "69452-309_2f9f880c-a70d-317b-e063-6294a90a2280", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "69452-309", "generic_name": "Prochlorperazine Maleate", "labeler_name": "Bionpharma Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PROCHLORPERAZINE MALEATE", "active_ingredients": [{"name": "PROCHLORPERAZINE MALEATE", "strength": "5 mg/1"}], "application_number": "ANDA217478", "marketing_category": "ANDA", "marketing_start_date": "20230913", "listing_expiration_date": "20261231"}