Package 50228-131-90

Brand: pramipexole dihydrochloride

Generic: pramipexole dihydrochloride
NDC Package

Package Facts

Identity

Package NDC 50228-131-90
Digits Only 5022813190
Product NDC 50228-131
Product ID 50228-131_14260a48-c15f-4517-9ce5-d26928b6a5f5
Description

90 TABLET in 1 BOTTLE (50228-131-90)

Marketing

Marketing Status
Marketed Since 2014-10-29
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": "14260a48-c15f-4517-9ce5-d26928b6a5f5", "openfda": {"upc": ["0350228131902", "0350228126106", "0350228129107", "0350228130103"], "unii": ["3D867NP06J"], "rxcui": ["858625", "859033", "859040", "859044", "859048", "859052"], "spl_set_id": ["395fee34-43dc-4840-a6b8-70d5736f9c8b"], "manufacturer_name": ["ScieGen Pharmaceuticals Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET in 1 BOTTLE (50228-131-10)", "package_ndc": "50228-131-10", "marketing_start_date": "20141029"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (50228-131-90)", "package_ndc": "50228-131-90", "marketing_start_date": "20141029"}], "brand_name": "Pramipexole Dihydrochloride", "product_id": "50228-131_14260a48-c15f-4517-9ce5-d26928b6a5f5", "dosage_form": "TABLET", "pharm_class": ["Dopamine Agonists [MoA]", "Nonergot Dopamine Agonist [EPC]"], "product_ndc": "50228-131", "generic_name": "Pramipexole Dihydrochloride", "labeler_name": "ScieGen Pharmaceuticals Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Pramipexole Dihydrochloride", "active_ingredients": [{"name": "PRAMIPEXOLE DIHYDROCHLORIDE", "strength": "1.5 mg/1"}], "application_number": "ANDA203855", "marketing_category": "ANDA", "marketing_start_date": "20141029", "listing_expiration_date": "20261231"}