Package 72189-216-60

Brand: primidone

Generic: primidone
NDC Package

Package Facts

Identity

Package NDC 72189-216-60
Digits Only 7218921660
Product NDC 72189-216
Product ID 72189-216_2be9877c-0b1e-23b4-e063-6394a90af68f
Description

60 TABLET in 1 BOTTLE (72189-216-60)

Marketing

Marketing Status
Marketed Since 2021-05-11
Brand primidone
Generic primidone
Sample Package No

Linked Drug Pages (1)

PRIMIDONE ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "2be9877c-0b1e-23b4-e063-6394a90af68f", "openfda": {"nui": ["N0000175753", "N0000008486"], "unii": ["13AFD7670Q"], "rxcui": ["198150"], "spl_set_id": ["c20f803c-e965-9dd8-e053-2995a90a92ba"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "pharm_class_epc": ["Anti-epileptic Agent [EPC]"], "manufacturer_name": ["DIRECT RX"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET in 1 BOTTLE (72189-216-60)", "package_ndc": "72189-216-60", "marketing_start_date": "20210511"}], "brand_name": "PRIMIDONE", "product_id": "72189-216_2be9877c-0b1e-23b4-e063-6394a90af68f", "dosage_form": "TABLET", "pharm_class": ["Anti-epileptic Agent [EPC]", "Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "72189-216", "generic_name": "PRIMIDONE", "labeler_name": "DIRECT RX", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PRIMIDONE", "active_ingredients": [{"name": "PRIMIDONE", "strength": "50 mg/1"}], "application_number": "ANDA040586", "marketing_category": "ANDA", "marketing_start_date": "20210511", "listing_expiration_date": "20261231"}