Package 55111-613-30

Brand: pramipexole dihydrochloride

Generic: pramipexole dihydrochloride
NDC Package

Package Facts

Identity

Package NDC 55111-613-30
Digits Only 5511161330
Product NDC 55111-613
Product ID 55111-613_4dfe5cc9-1281-c6dc-a6dc-6113fd0aed67
Description

30 TABLET, EXTENDED RELEASE in 1 BOTTLE (55111-613-30)

Marketing

Marketing Status
Marketed Since 2015-08-14
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": "4dfe5cc9-1281-c6dc-a6dc-6113fd0aed67", "openfda": {"unii": ["3D867NP06J"], "rxcui": ["901546", "901550", "901555", "901534", "901541"], "spl_set_id": ["00699692-532a-68fd-8a51-3770a81b2208"], "manufacturer_name": ["Dr. Reddy's Laboratories Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (55111-613-30)", "package_ndc": "55111-613-30", "marketing_start_date": "20150814"}], "brand_name": "Pramipexole dihydrochloride", "product_id": "55111-613_4dfe5cc9-1281-c6dc-a6dc-6113fd0aed67", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Dopamine Agonists [MoA]", "Nonergot Dopamine Agonist [EPC]"], "product_ndc": "55111-613", "generic_name": "Pramipexole dihydrochloride", "labeler_name": "Dr. Reddy's Laboratories Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Pramipexole dihydrochloride", "active_ingredients": [{"name": "PRAMIPEXOLE DIHYDROCHLORIDE", "strength": "1.5 mg/1"}], "application_number": "ANDA203354", "marketing_category": "ANDA", "marketing_start_date": "20150814", "listing_expiration_date": "20261231"}