Package 46708-578-30

Brand: pramipexole dihydrochloride

Generic: pramipexole dihydrochloride
NDC Package

Package Facts

Identity

Package NDC 46708-578-30
Digits Only 4670857830
Product NDC 46708-578
Product ID 46708-578_c9aa6022-4a1b-4fd5-a7ba-04158d9b5a05
Description

30 TABLET, EXTENDED RELEASE in 1 BOTTLE (46708-578-30)

Marketing

Marketing Status
Marketed Since 2019-01-03
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": "c9aa6022-4a1b-4fd5-a7ba-04158d9b5a05", "openfda": {"upc": ["0346708574307", "0346708579302", "0346708578305", "0346708575304", "0346708576301"], "unii": ["3D867NP06J"], "rxcui": ["901534", "901541", "901546", "901550", "901555", "1114479", "1114485"], "spl_set_id": ["b6935240-ee81-49ef-adad-fb900d7f5127"], "manufacturer_name": ["Alembic Pharmaceuticals Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (46708-578-30)", "package_ndc": "46708-578-30", "marketing_start_date": "20190103"}], "brand_name": "Pramipexole Dihydrochloride", "product_id": "46708-578_c9aa6022-4a1b-4fd5-a7ba-04158d9b5a05", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Dopamine Agonists [MoA]", "Nonergot Dopamine Agonist [EPC]"], "product_ndc": "46708-578", "generic_name": "Pramipexole Dihydrochloride", "labeler_name": "Alembic Pharmaceuticals Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Pramipexole Dihydrochloride", "active_ingredients": [{"name": "PRAMIPEXOLE DIHYDROCHLORIDE", "strength": "3 mg/1"}], "application_number": "ANDA204518", "marketing_category": "ANDA", "marketing_start_date": "20190103", "listing_expiration_date": "20261231"}