Package 50090-5036-0

Brand: pramipexole dihydrochloride

Generic: pramipexole dihydrochloride
NDC Package

Package Facts

Identity

Package NDC 50090-5036-0
Digits Only 5009050360
Product NDC 50090-5036
Product ID 50090-5036_32458c95-4cff-4b30-bc62-0f0b2203a584
Description

90 TABLET in 1 BOTTLE (50090-5036-0)

Marketing

Marketing Status
Marketed Since 2020-05-06
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": "32458c95-4cff-4b30-bc62-0f0b2203a584", "openfda": {"unii": ["3D867NP06J"], "rxcui": ["859048"], "spl_set_id": ["7cd6a546-d516-427c-af79-555390ccd35b"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (50090-5036-0)", "package_ndc": "50090-5036-0", "marketing_start_date": "20200506"}], "brand_name": "Pramipexole Dihydrochloride", "product_id": "50090-5036_32458c95-4cff-4b30-bc62-0f0b2203a584", "dosage_form": "TABLET", "pharm_class": ["Dopamine Agonists [MoA]", "Nonergot Dopamine Agonist [EPC]"], "product_ndc": "50090-5036", "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": "1.5 mg/1"}], "application_number": "ANDA202633", "marketing_category": "ANDA", "marketing_start_date": "20121026", "listing_expiration_date": "20261231"}