Package 0904-6704-61

Brand: pramipexole dihydrochloride

Generic: pramipexole dihydrochloride
NDC Package

Package Facts

Identity

Package NDC 0904-6704-61
Digits Only 0904670461
Product NDC 0904-6704
Description

100 BLISTER PACK in 1 CARTON (0904-6704-61) / 1 TABLET in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2010-10-08
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": "9ad8df87-b8f1-4a39-a391-d7f7548de896", "openfda": {"unii": ["3D867NP06J"], "rxcui": ["859040"], "spl_set_id": ["978c0e89-35f0-44a2-9302-8bed7e5d60e0"], "manufacturer_name": ["Major Pharmaceuticals"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 CARTON (0904-6704-61)  / 1 TABLET in 1 BLISTER PACK", "package_ndc": "0904-6704-61", "marketing_start_date": "20101008"}], "brand_name": "Pramipexole Dihydrochloride", "product_id": "0904-6704_9ad8df87-b8f1-4a39-a391-d7f7548de896", "dosage_form": "TABLET", "pharm_class": ["Dopamine Agonists [MoA]", "Nonergot Dopamine Agonist [EPC]"], "product_ndc": "0904-6704", "generic_name": "Pramipexole Dihydrochloride", "labeler_name": "Major Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Pramipexole Dihydrochloride", "active_ingredients": [{"name": "PRAMIPEXOLE DIHYDROCHLORIDE", "strength": ".25 mg/1"}], "application_number": "ANDA090865", "marketing_category": "ANDA", "marketing_start_date": "20101008", "listing_expiration_date": "20271231"}