Package 60687-581-21

Brand: pramipexole dihydrochloride

Generic: pramipexole dihydrochloride
NDC Package

Package Facts

Identity

Package NDC 60687-581-21
Digits Only 6068758121
Product NDC 60687-581
Description

30 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-581-21) / 1 TABLET in 1 BLISTER PACK (60687-581-11)

Marketing

Marketing Status
Marketed Since 2020-08-13
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": "4c252238-7629-b19d-e063-6294a90a4c38", "openfda": {"unii": ["3D867NP06J"], "rxcui": ["859040", "859044", "859052"], "spl_set_id": ["f4d97c2e-f447-4cfe-b9d4-852323f0cfb5"], "manufacturer_name": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "30 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-581-21)  / 1 TABLET in 1 BLISTER PACK (60687-581-11)", "package_ndc": "60687-581-21", "marketing_start_date": "20200813"}], "brand_name": "Pramipexole Dihydrochloride", "product_id": "60687-581_4c252238-7629-b19d-e063-6294a90a4c38", "dosage_form": "TABLET", "pharm_class": ["Dopamine Agonists [MoA]", "Nonergot Dopamine Agonist [EPC]"], "product_ndc": "60687-581", "generic_name": "Pramipexole Dihydrochloride", "labeler_name": "American Health Packaging", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Pramipexole Dihydrochloride", "active_ingredients": [{"name": "PRAMIPEXOLE DIHYDROCHLORIDE", "strength": ".5 mg/1"}], "application_number": "ANDA090865", "marketing_category": "ANDA", "marketing_start_date": "20200813", "listing_expiration_date": "20271231"}