Package 16714-922-01

Brand: pramipexole dihydrochloride

Generic: pramipexole dihydrochloride
NDC Package

Package Facts

Identity

Package NDC 16714-922-01
Digits Only 1671492201
Product NDC 16714-922
Product ID 16714-922_b78c4a9c-3ad8-443e-ada5-853385411cfc
Description

30 TABLET, EXTENDED RELEASE in 1 BOTTLE (16714-922-01)

Marketing

Marketing Status
Marketed Since 2019-03-06
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": "b78c4a9c-3ad8-443e-ada5-853385411cfc", "openfda": {"unii": ["3D867NP06J"], "rxcui": ["901534", "901541", "901546", "901550", "901555", "1114479"], "spl_set_id": ["946c8a72-8c48-4925-93d3-7940f4c0fd29"], "manufacturer_name": ["NorthStar RxLLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (16714-922-01)", "package_ndc": "16714-922-01", "marketing_start_date": "20190306"}], "brand_name": "Pramipexole Dihydrochloride", "product_id": "16714-922_b78c4a9c-3ad8-443e-ada5-853385411cfc", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Dopamine Agonists [MoA]", "Nonergot Dopamine Agonist [EPC]"], "product_ndc": "16714-922", "generic_name": "Pramipexole Dihydrochloride", "labeler_name": "NorthStar RxLLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Pramipexole Dihydrochloride", "active_ingredients": [{"name": "PRAMIPEXOLE DIHYDROCHLORIDE", "strength": "4.5 mg/1"}], "application_number": "ANDA206156", "marketing_category": "ANDA", "marketing_start_date": "20190306", "listing_expiration_date": "20261231"}