Package 69452-472-32

Brand: prochlorperazine maleate

Generic: prochlorperazine maleate
NDC Package

Package Facts

Identity

Package NDC 69452-472-32
Digits Only 6945247232
Product NDC 69452-472
Description

1000 TABLET in 1 BOTTLE (69452-472-32)

Marketing

Marketing Status
Marketed Since 2025-01-31
Brand prochlorperazine maleate
Generic prochlorperazine maleate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2cf363d6-b9e5-2c22-e063-6394a90a7649", "openfda": {"unii": ["I1T8O1JTL6"], "rxcui": ["198365", "312635"], "spl_set_id": ["2cf363d6-b9e4-2c22-e063-6394a90a7649"], "manufacturer_name": ["Bionpharma Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (69452-472-20)", "package_ndc": "69452-472-20", "marketing_start_date": "20250131"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (69452-472-32)", "package_ndc": "69452-472-32", "marketing_start_date": "20250131"}], "brand_name": "PROCHLORPERAZINE MALEATE", "product_id": "69452-472_2cf363d6-b9e5-2c22-e063-6394a90a7649", "dosage_form": "TABLET", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "69452-472", "generic_name": "Prochlorperazine Maleate", "labeler_name": "Bionpharma Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PROCHLORPERAZINE MALEATE", "active_ingredients": [{"name": "PROCHLORPERAZINE MALEATE", "strength": "10 mg/1"}], "application_number": "ANDA217478", "marketing_category": "ANDA", "marketing_start_date": "20250131", "listing_expiration_date": "20261231"}