Package 72162-2569-9

Brand: pramipexole dihydrochloride

Generic: pramipexole dihydrochloride
NDC Package

Package Facts

Identity

Package NDC 72162-2569-9
Digits Only 7216225699
Product NDC 72162-2569
Product ID 72162-2569_d1b4c9db-7f4e-4a80-997f-c0d7bcbb04a1
Description

90 TABLET in 1 BOTTLE (72162-2569-9)

Marketing

Marketing Status
Marketed Since 2025-11-17
Brand pramipexole dihydrochloride
Generic pramipexole dihydrochloride
Sample Package No

Linked Drug Pages (1)

Pramipexole Dihydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "d1b4c9db-7f4e-4a80-997f-c0d7bcbb04a1", "openfda": {"unii": ["3D867NP06J"], "rxcui": ["858625"], "spl_set_id": ["794fdab8-1c15-4469-963e-4f9e3495536f"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (72162-2569-9)", "package_ndc": "72162-2569-9", "marketing_start_date": "20251117"}], "brand_name": "Pramipexole Dihydrochloride", "product_id": "72162-2569_d1b4c9db-7f4e-4a80-997f-c0d7bcbb04a1", "dosage_form": "TABLET", "pharm_class": ["Dopamine Agonists [MoA]", "Nonergot Dopamine Agonist [EPC]"], "product_ndc": "72162-2569", "generic_name": "Pramipexole Dihydrochloride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Pramipexole Dihydrochloride", "active_ingredients": [{"name": "PRAMIPEXOLE DIHYDROCHLORIDE", "strength": ".75 mg/1"}], "application_number": "ANDA090865", "marketing_category": "ANDA", "marketing_start_date": "20101008", "listing_expiration_date": "20261231"}