Package 0527-1231-01

Brand: primidone

Generic: primidone
NDC Package

Package Facts

Identity

Package NDC 0527-1231-01
Digits Only 0527123101
Product NDC 0527-1231
Description

100 TABLET in 1 BOTTLE (0527-1231-01)

Marketing

Marketing Status
Marketed Since 1978-12-01
Brand primidone
Generic primidone
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "99bd0a67-2742-43dd-9ddc-430b9141c3b1", "openfda": {"nui": ["N0000175753", "N0000008486"], "upc": ["0305871231011"], "unii": ["13AFD7670Q"], "rxcui": ["96304", "198150"], "spl_set_id": ["a1a817f7-c190-4825-94eb-442f477187e3"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "pharm_class_epc": ["Anti-epileptic Agent [EPC]"], "manufacturer_name": ["Lannett Company, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (0527-1231-01)", "package_ndc": "0527-1231-01", "marketing_start_date": "19781201"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (0527-1231-05)", "package_ndc": "0527-1231-05", "marketing_start_date": "19781201"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (0527-1231-10)", "package_ndc": "0527-1231-10", "marketing_start_date": "19781201"}], "brand_name": "Primidone", "product_id": "0527-1231_99bd0a67-2742-43dd-9ddc-430b9141c3b1", "dosage_form": "TABLET", "pharm_class": ["Anti-epileptic Agent [EPC]", "Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "0527-1231", "generic_name": "Primidone", "labeler_name": "Lannett Company, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Primidone", "active_ingredients": [{"name": "PRIMIDONE", "strength": "250 mg/1"}], "application_number": "ANDA084903", "marketing_category": "ANDA", "marketing_start_date": "19781201", "listing_expiration_date": "20261231"}