Package 0615-8551-39

Brand: pramipexole dihydrochloride

Generic: pramipexole dihydrochloride
NDC Package

Package Facts

Identity

Package NDC 0615-8551-39
Digits Only 0615855139
Product NDC 0615-8551
Product ID 0615-8551_7d36ceb3-2235-42bc-bb8c-e7863c24b1cb
Description

30 TABLET in 1 BLISTER PACK (0615-8551-39)

Marketing

Marketing Status
Marketed Since 2024-10-07
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": "7d36ceb3-2235-42bc-bb8c-e7863c24b1cb", "openfda": {"unii": ["3D867NP06J"], "rxcui": ["859040", "859044"], "spl_set_id": ["5e6f2187-a5cc-481e-b0a1-d38d3f92e822"], "manufacturer_name": ["NCS HealthCare of KY, LLC dba Vangard Labs"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (0615-8551-39)", "package_ndc": "0615-8551-39", "marketing_start_date": "20241007"}], "brand_name": "Pramipexole dihydrochloride", "product_id": "0615-8551_7d36ceb3-2235-42bc-bb8c-e7863c24b1cb", "dosage_form": "TABLET", "pharm_class": ["Dopamine Agonists [MoA]", "Nonergot Dopamine Agonist [EPC]"], "product_ndc": "0615-8551", "generic_name": "Pramipexole dihydrochloride", "labeler_name": "NCS HealthCare of KY, LLC dba Vangard Labs", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Pramipexole dihydrochloride", "active_ingredients": [{"name": "PRAMIPEXOLE DIHYDROCHLORIDE", "strength": ".25 mg/1"}], "application_number": "ANDA090781", "marketing_category": "ANDA", "marketing_start_date": "20101008", "listing_expiration_date": "20261231"}