Package 63629-8289-1

Brand: pramipexole dihydrochloride

Generic: pramipexole dihydrochloride
NDC Package

Package Facts

Identity

Package NDC 63629-8289-1
Digits Only 6362982891
Product NDC 63629-8289
Product ID 63629-8289_e0c596d9-a2a0-42bd-a987-7d3d8df3488b
Description

30 TABLET in 1 BOTTLE (63629-8289-1)

Marketing

Marketing Status
Marketed Since 2020-01-10
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": "e0c596d9-a2a0-42bd-a987-7d3d8df3488b", "openfda": {"unii": ["3D867NP06J"], "rxcui": ["859052"], "spl_set_id": ["1ebb3e0b-8fd5-4ac8-ba2f-abfcfc0c91ad"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (63629-8289-1)", "package_ndc": "63629-8289-1", "marketing_start_date": "20200110"}], "brand_name": "Pramipexole Dihydrochloride", "product_id": "63629-8289_e0c596d9-a2a0-42bd-a987-7d3d8df3488b", "dosage_form": "TABLET", "pharm_class": ["Dopamine Agonists [MoA]", "Nonergot Dopamine Agonist [EPC]"], "product_ndc": "63629-8289", "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": "1 mg/1"}], "application_number": "ANDA202633", "marketing_category": "ANDA", "marketing_start_date": "20121026", "listing_expiration_date": "20261231"}