Package 69367-694-01

Brand: phenobarbital

Generic: phenobarbital
NDC Package

Package Facts

Identity

Package NDC 69367-694-01
Digits Only 6936769401
Product NDC 69367-694
Description

100 TABLET in 1 BOTTLE (69367-694-01)

Marketing

Marketing Status
Marketed Since 2023-09-08
Brand phenobarbital
Generic phenobarbital
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "b8256561-2c8d-4b02-8a59-5fbc524e4eb3", "openfda": {"upc": ["0369367692014", "0369367693011", "0369367694018", "0369367691017"], "unii": ["YQE403BP4D"], "rxcui": ["198083", "198089", "312357", "312362"], "spl_set_id": ["4e70d33b-82f3-4a8e-a35b-ee658b3e0ab1"], "manufacturer_name": ["Westminster Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (69367-694-01)", "package_ndc": "69367-694-01", "marketing_start_date": "20230908"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (69367-694-05)", "package_ndc": "69367-694-05", "marketing_start_date": "20230908"}], "brand_name": "Phenobarbital", "product_id": "69367-694_b8256561-2c8d-4b02-8a59-5fbc524e4eb3", "dosage_form": "TABLET", "product_ndc": "69367-694", "dea_schedule": "CIV", "generic_name": "Phenobarbital", "labeler_name": "Westminster Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Phenobarbital", "active_ingredients": [{"name": "PHENOBARBITAL", "strength": "100 mg/1"}], "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "20230908", "listing_expiration_date": "20261231"}