Package 16571-225-01

Brand: timolol maleate

Generic: timolol maleate
NDC Package

Package Facts

Identity

Package NDC 16571-225-01
Digits Only 1657122501
Product NDC 16571-225
Description

100 TABLET in 1 BOTTLE (16571-225-01)

Marketing

Marketing Status
Marketed Since 2024-12-10
Brand timolol maleate
Generic timolol maleate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "ebb620d8-8e2e-4632-b8a8-74f41c9969e6", "openfda": {"unii": ["P8Y54F701R"], "rxcui": ["198284", "198285", "198286"], "spl_set_id": ["0bc40b2c-65eb-4095-87e6-4752d5b19a3a"], "manufacturer_name": ["Rising Pharma Holdings, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (16571-225-01)", "package_ndc": "16571-225-01", "marketing_start_date": "20241210"}], "brand_name": "Timolol Maleate", "product_id": "16571-225_ebb620d8-8e2e-4632-b8a8-74f41c9969e6", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "16571-225", "generic_name": "Timolol Maleate", "labeler_name": "Rising Pharma Holdings, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Timolol Maleate", "active_ingredients": [{"name": "TIMOLOL MALEATE", "strength": "20 mg/1"}], "application_number": "ANDA207556", "marketing_category": "ANDA", "marketing_start_date": "20241210", "listing_expiration_date": "20261231"}