Package 71335-2167-1

Brand: pramipexole dihydrochloride

Generic: pramipexole dihydrochloride
NDC Package

Package Facts

Identity

Package NDC 71335-2167-1
Digits Only 7133521671
Product NDC 71335-2167
Product ID 71335-2167_64bc0137-ae12-4d44-8934-a0b9029e97c0
Description

30 TABLET in 1 BOTTLE (71335-2167-1)

Marketing

Marketing Status
Marketed Since 2022-09-01
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": "64bc0137-ae12-4d44-8934-a0b9029e97c0", "openfda": {"unii": ["3D867NP06J"], "rxcui": ["859052"], "spl_set_id": ["46f88017-7b0e-437e-90b1-37bdf9013e72"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (71335-2167-1)", "package_ndc": "71335-2167-1", "marketing_start_date": "20220901"}], "brand_name": "Pramipexole Dihydrochloride", "product_id": "71335-2167_64bc0137-ae12-4d44-8934-a0b9029e97c0", "dosage_form": "TABLET", "pharm_class": ["Dopamine Agonists [MoA]", "Nonergot Dopamine Agonist [EPC]"], "product_ndc": "71335-2167", "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": "ANDA090865", "marketing_category": "ANDA", "marketing_start_date": "20101008", "listing_expiration_date": "20261231"}