Package 69680-146-30
Brand: pramipexole dihydrochloride
Generic: pramipexole dihydrochloridePackage Facts
Identity
Package NDC
69680-146-30
Digits Only
6968014630
Product NDC
69680-146
Description
30 TABLET, EXTENDED RELEASE in 1 BOTTLE (69680-146-30)
Marketing
Marketing Status
Brand
pramipexole dihydrochloride
Generic
pramipexole dihydrochloride
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "232ae12c-b9bc-4ca7-982e-d6f43b6c8eec", "openfda": {"upc": ["0369680145303", "0369680146300"], "unii": ["3D867NP06J"], "rxcui": ["901541", "901546"], "spl_set_id": ["d07aad1b-e078-4fca-8386-ca2e8e899688"], "manufacturer_name": ["Vitruvias Therapeutics, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (69680-146-30)", "package_ndc": "69680-146-30", "marketing_start_date": "20210827"}], "brand_name": "Pramipexole Dihydrochloride", "product_id": "69680-146_232ae12c-b9bc-4ca7-982e-d6f43b6c8eec", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Dopamine Agonists [MoA]", "Nonergot Dopamine Agonist [EPC]"], "product_ndc": "69680-146", "generic_name": "Pramipexole Dihydrochloride", "labeler_name": "Vitruvias Therapeutics, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Pramipexole Dihydrochloride", "active_ingredients": [{"name": "PRAMIPEXOLE DIHYDROCHLORIDE", "strength": ".75 mg/1"}], "application_number": "ANDA212797", "marketing_category": "ANDA", "marketing_start_date": "20210827", "listing_expiration_date": "20261231"}