Package 69367-367-16

Brand: phenobarbital

Generic: phenobarbital
NDC Package

Package Facts

Identity

Package NDC 69367-367-16
Digits Only 6936736716
Product NDC 69367-367
Product ID 69367-367_cf0962ad-4f57-4733-a836-844ac7764a01
Description

473 mL in 1 BOTTLE, PLASTIC (69367-367-16)

Marketing

Marketing Status
Marketed Since 2025-05-01
Brand phenobarbital
Generic phenobarbital
Sample Package No

Linked Drug Pages (1)

Phenobarbital ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "cf0962ad-4f57-4733-a836-844ac7764a01", "openfda": {"upc": ["0369367367165"], "unii": ["YQE403BP4D"], "rxcui": ["702519"], "spl_set_id": ["87148299-a3a6-40af-afa6-f32ac2f678c6"], "manufacturer_name": ["Westminster Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "473 mL in 1 BOTTLE, PLASTIC (69367-367-16)", "package_ndc": "69367-367-16", "marketing_start_date": "20250501"}], "brand_name": "Phenobarbital", "product_id": "69367-367_cf0962ad-4f57-4733-a836-844ac7764a01", "dosage_form": "ELIXIR", "product_ndc": "69367-367", "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": "20 mg/5mL"}], "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "20250501", "listing_expiration_date": "20261231"}