Package 59651-773-01

Brand: prochlorperazine maleate

Generic: prochlorperazine maleate
NDC Package

Package Facts

Identity

Package NDC 59651-773-01
Digits Only 5965177301
Product NDC 59651-773
Product ID 59651-773_7ec4df20-9ea5-4a68-a43f-5ded4eaed235
Description

100 TABLET, FILM COATED in 1 BOTTLE (59651-773-01)

Marketing

Marketing Status
Marketed Since 2025-09-08
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": "7ec4df20-9ea5-4a68-a43f-5ded4eaed235", "openfda": {"unii": ["I1T8O1JTL6"], "rxcui": ["198365", "312635"], "spl_set_id": ["7ec4df20-9ea5-4a68-a43f-5ded4eaed235"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (59651-773-01)", "package_ndc": "59651-773-01", "marketing_start_date": "20250908"}], "brand_name": "prochlorperazine maleate", "product_id": "59651-773_7ec4df20-9ea5-4a68-a43f-5ded4eaed235", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "59651-773", "generic_name": "prochlorperazine maleate", "labeler_name": "Aurobindo Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "prochlorperazine maleate", "active_ingredients": [{"name": "PROCHLORPERAZINE MALEATE", "strength": "5 mg/1"}], "application_number": "ANDA218734", "marketing_category": "ANDA", "marketing_start_date": "20250908", "listing_expiration_date": "20261231"}