Package 71335-1537-1

Brand: pramipexole dihydrochloride

Generic: pramipexole dihydrochloride
NDC Package

Package Facts

Identity

Package NDC 71335-1537-1
Digits Only 7133515371
Product NDC 71335-1537
Description

30 TABLET in 1 BOTTLE (71335-1537-1)

Marketing

Marketing Status
Marketed Since 2020-03-16
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": "29f9b38b-000e-4f65-8e28-3c77c3caaa76", "openfda": {"unii": ["3D867NP06J"], "rxcui": ["859033"], "spl_set_id": ["468830df-941c-4363-b432-94de9b7fd2ac"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (71335-1537-1)", "package_ndc": "71335-1537-1", "marketing_start_date": "20200316"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (71335-1537-2)", "package_ndc": "71335-1537-2", "marketing_start_date": "20211123"}], "brand_name": "Pramipexole Dihydrochloride", "product_id": "71335-1537_29f9b38b-000e-4f65-8e28-3c77c3caaa76", "dosage_form": "TABLET", "pharm_class": ["Dopamine Agonists [MoA]", "Nonergot Dopamine Agonist [EPC]"], "product_ndc": "71335-1537", "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": "ANDA202633", "marketing_category": "ANDA", "marketing_start_date": "20121026", "listing_expiration_date": "20261231"}