Package 72189-503-30

Brand: prochlorperazine maleate

Generic: prochlorperazine maleate
NDC Package

Package Facts

Identity

Package NDC 72189-503-30
Digits Only 7218950330
Product NDC 72189-503
Product ID 72189-503_2c4e4a5c-f12a-8c46-e063-6394a90ae95e
Description

30 TABLET in 1 BOTTLE (72189-503-30)

Marketing

Marketing Status
Marketed Since 2023-08-03
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": "2c4e4a5c-f12a-8c46-e063-6394a90ae95e", "openfda": {"unii": ["I1T8O1JTL6"], "rxcui": ["198365"], "spl_set_id": ["02069e43-5245-20dc-e063-6294a90a9dcd"], "manufacturer_name": ["Direct_Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (72189-503-30)", "package_ndc": "72189-503-30", "marketing_start_date": "20230803"}], "brand_name": "Prochlorperazine Maleate", "product_id": "72189-503_2c4e4a5c-f12a-8c46-e063-6394a90ae95e", "dosage_form": "TABLET", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "72189-503", "generic_name": "Prochlorperazine Maleate", "labeler_name": "Direct_Rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Prochlorperazine Maleate", "active_ingredients": [{"name": "PROCHLORPERAZINE MALEATE", "strength": "10 mg/1"}], "application_number": "ANDA040268", "marketing_category": "ANDA", "marketing_start_date": "20230803", "listing_expiration_date": "20261231"}