Package 69452-472-32
Brand: prochlorperazine maleate
Generic: prochlorperazine maleatePackage 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
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"}