Package 50090-3280-0

Brand: pramipexole dihydrochloride

Generic: pramipexole dihydrochloride
NDC Package

Package Facts

Identity

Package NDC 50090-3280-0
Digits Only 5009032800
Product NDC 50090-3280
Product ID 50090-3280_f192c472-528a-4328-ac85-1e2c27eb8c78
Description

90 TABLET in 1 BOTTLE (50090-3280-0)

Marketing

Marketing Status
Marketed Since 2017-11-27
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": "f192c472-528a-4328-ac85-1e2c27eb8c78", "openfda": {"unii": ["3D867NP06J"], "rxcui": ["859040", "859044"], "spl_set_id": ["29b639e3-25a5-4c2f-b4ea-a119db79fe0c"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (50090-3280-0)", "package_ndc": "50090-3280-0", "marketing_start_date": "20171127"}], "brand_name": "Pramipexole Dihydrochloride", "product_id": "50090-3280_f192c472-528a-4328-ac85-1e2c27eb8c78", "dosage_form": "TABLET", "pharm_class": ["Dopamine Agonists [MoA]", "Nonergot Dopamine Agonist [EPC]"], "product_ndc": "50090-3280", "generic_name": "Pramipexole Dihydrochloride", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Pramipexole Dihydrochloride", "active_ingredients": [{"name": "PRAMIPEXOLE DIHYDROCHLORIDE", "strength": ".25 mg/1"}], "application_number": "ANDA202633", "marketing_category": "ANDA", "marketing_start_date": "20121026", "listing_expiration_date": "20261231"}