Package 72603-169-01

Brand: prochlorperazine maleate

Generic: prochlorperazine maleate
NDC Package

Package Facts

Identity

Package NDC 72603-169-01
Digits Only 7260316901
Product NDC 72603-169
Product ID 72603-169_2dda6392-975a-4d77-e063-6294a90a2f67
Description

100 TABLET in 1 BOTTLE (72603-169-01)

Marketing

Marketing Status
Marketed Since 2023-09-07
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": "2dda6392-975a-4d77-e063-6294a90a2f67", "openfda": {"unii": ["I1T8O1JTL6"], "rxcui": ["198365", "312635"], "spl_set_id": ["04bf8a16-218a-c648-e063-6294a90a1afb"], "manufacturer_name": ["Northstar Rx LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (72603-169-01)", "package_ndc": "72603-169-01", "marketing_start_date": "20230907"}], "brand_name": "Prochlorperazine Maleate", "product_id": "72603-169_2dda6392-975a-4d77-e063-6294a90a2f67", "dosage_form": "TABLET", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "72603-169", "generic_name": "Prochlorperazine Maleate", "labeler_name": "Northstar Rx LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Prochlorperazine Maleate", "active_ingredients": [{"name": "PROCHLORPERAZINE MALEATE", "strength": "10 mg/1"}], "application_number": "ANDA216202", "marketing_category": "ANDA", "marketing_start_date": "20230907", "listing_expiration_date": "20261231"}