Package 46708-615-90
Brand: pramipexole dihydrochloride
Generic: pramipexole dihydrochloridePackage Facts
Identity
Package NDC
46708-615-90
Digits Only
4670861590
Product NDC
46708-615
Description
90 TABLET in 1 BOTTLE (46708-615-90)
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": "43b3cc2f-5e67-4440-a896-69f9be384e33", "openfda": {"upc": ["0346708614904", "0346708615901", "0346708613907", "0346708611903"], "unii": ["3D867NP06J"], "rxcui": ["859033", "859040", "859044", "859048", "859052"], "spl_set_id": ["0a3ed933-ef5b-4091-8ae9-5768ae18514f"], "manufacturer_name": ["Alembic Pharmaceuticals Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (46708-615-90)", "package_ndc": "46708-615-90", "marketing_start_date": "20160322"}], "brand_name": "Pramipexole Dihydrochloride", "product_id": "46708-615_43b3cc2f-5e67-4440-a896-69f9be384e33", "dosage_form": "TABLET", "pharm_class": ["Dopamine Agonists [MoA]", "Nonergot Dopamine Agonist [EPC]"], "product_ndc": "46708-615", "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": "1.5 mg/1"}], "application_number": "ANDA078894", "marketing_category": "ANDA", "marketing_start_date": "20160322", "listing_expiration_date": "20261231"}