Package 63629-5042-2

Brand: pramipexole dihydrochloride

Generic: pramipexole dihydrochloride
NDC Package

Package Facts

Identity

Package NDC 63629-5042-2
Digits Only 6362950422
Product NDC 63629-5042
Description

60 TABLET in 1 BOTTLE (63629-5042-2)

Marketing

Marketing Status
Marketed Since 2013-09-10
Brand pramipexole dihydrochloride
Generic pramipexole dihydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3108c6c7-7c35-47f6-9f16-69c2e9e8decb", "openfda": {"unii": ["3D867NP06J"], "rxcui": ["859033"], "spl_set_id": ["bd0f7ae1-11ef-4fab-894f-c4c59f75aa99"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (63629-5042-1)", "package_ndc": "63629-5042-1", "marketing_start_date": "20130716"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (63629-5042-2)", "package_ndc": "63629-5042-2", "marketing_start_date": "20130910"}], "brand_name": "Pramipexole Dihydrochloride", "product_id": "63629-5042_3108c6c7-7c35-47f6-9f16-69c2e9e8decb", "dosage_form": "TABLET", "pharm_class": ["Dopamine Agonists [MoA]", "Nonergot Dopamine Agonist [EPC]"], "product_ndc": "63629-5042", "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": ".125 mg/1"}], "application_number": "ANDA090865", "marketing_category": "ANDA", "marketing_start_date": "20101008", "listing_expiration_date": "20261231"}