Package 57237-183-90

Brand: pramipexole dihydrochloride

Generic: pramipexole dihydrochloride
NDC Package

Package Facts

Identity

Package NDC 57237-183-90
Digits Only 5723718390
Product NDC 57237-183
Product ID 57237-183_967cfcd5-d04f-4637-a364-632bf7ca72b8
Description

90 TABLET in 1 BOTTLE (57237-183-90)

Marketing

Marketing Status
Marketed Since 2012-10-26
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": "967cfcd5-d04f-4637-a364-632bf7ca72b8", "openfda": {"upc": ["0357237182901", "0357237180907", "0357237181904"], "unii": ["3D867NP06J"], "rxcui": ["858625", "859033", "859040", "859044", "859048", "859052"], "spl_set_id": ["56e8d1f6-6dbf-4e11-a177-a56bbfb9f8ec"], "manufacturer_name": ["Rising Pharma Holdings, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (57237-183-90)", "package_ndc": "57237-183-90", "marketing_start_date": "20121026"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (57237-183-99)", "package_ndc": "57237-183-99", "marketing_start_date": "20121026"}], "brand_name": "Pramipexole Dihydrochloride", "product_id": "57237-183_967cfcd5-d04f-4637-a364-632bf7ca72b8", "dosage_form": "TABLET", "pharm_class": ["Dopamine Agonists [MoA]", "Nonergot Dopamine Agonist [EPC]"], "product_ndc": "57237-183", "generic_name": "Pramipexole Dihydrochloride", "labeler_name": "Rising Pharma Holdings, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Pramipexole Dihydrochloride", "active_ingredients": [{"name": "PRAMIPEXOLE DIHYDROCHLORIDE", "strength": ".75 mg/1"}], "application_number": "ANDA202633", "marketing_category": "ANDA", "marketing_start_date": "20121026", "listing_expiration_date": "20271231"}