Package 65862-604-90
Brand: pramipexole dihydrochloride
Generic: pramipexole dihydrochloridePackage Facts
Identity
Package NDC
65862-604-90
Digits Only
6586260490
Product NDC
65862-604
Description
90 TABLET in 1 BOTTLE (65862-604-90)
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": "1e01cf5f-29b7-40ce-8c46-40f8dc65ce3e", "openfda": {"upc": ["0365862604903"], "unii": ["3D867NP06J"], "rxcui": ["858625", "859033", "859040", "859044", "859048", "859052"], "spl_set_id": ["3f90971a-e005-4dd3-bb93-b09125ada3c8"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 BLISTER PACK in 1 CARTON (65862-604-78) / 10 TABLET in 1 BLISTER PACK (65862-604-10)", "package_ndc": "65862-604-78", "marketing_start_date": "20121026"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (65862-604-90)", "package_ndc": "65862-604-90", "marketing_start_date": "20121026"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (65862-604-99)", "package_ndc": "65862-604-99", "marketing_start_date": "20121026"}], "brand_name": "Pramipexole Dihydrochloride", "product_id": "65862-604_1e01cf5f-29b7-40ce-8c46-40f8dc65ce3e", "dosage_form": "TABLET", "pharm_class": ["Dopamine Agonists [MoA]", "Nonergot Dopamine Agonist [EPC]"], "product_ndc": "65862-604", "generic_name": "Pramipexole Dihydrochloride", "labeler_name": "Aurobindo Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Pramipexole Dihydrochloride", "active_ingredients": [{"name": "PRAMIPEXOLE DIHYDROCHLORIDE", "strength": ".125 mg/1"}], "application_number": "ANDA202633", "marketing_category": "ANDA", "marketing_start_date": "20121026", "listing_expiration_date": "20261231"}