Package 71335-1504-2
Brand: pramipexole dihydrochloride
Generic: pramipexole dihydrochloridePackage Facts
Identity
Package NDC
71335-1504-2
Digits Only
7133515042
Product NDC
71335-1504
Description
90 TABLET in 1 BOTTLE (71335-1504-2)
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": "b9f0ffda-1cd2-47c8-85f5-3e61a567f207", "openfda": {"unii": ["3D867NP06J"], "rxcui": ["859048"], "spl_set_id": ["422b27af-5e7d-4fe1-81bc-ed545c26b476"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (71335-1504-1)", "package_ndc": "71335-1504-1", "marketing_start_date": "20211228"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71335-1504-2)", "package_ndc": "71335-1504-2", "marketing_start_date": "20200211"}], "brand_name": "Pramipexole Dihydrochloride", "product_id": "71335-1504_b9f0ffda-1cd2-47c8-85f5-3e61a567f207", "dosage_form": "TABLET", "pharm_class": ["Dopamine Agonists [MoA]", "Nonergot Dopamine Agonist [EPC]"], "product_ndc": "71335-1504", "generic_name": "Pramipexole Dihydrochloride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Pramipexole Dihydrochloride", "active_ingredients": [{"name": "PRAMIPEXOLE DIHYDROCHLORIDE", "strength": "1.5 mg/1"}], "application_number": "ANDA202633", "marketing_category": "ANDA", "marketing_start_date": "20121026", "listing_expiration_date": "20261231"}