Package 69367-357-16

Brand: phenobarbital

Generic: phenobarbital
NDC Package

Package Facts

Identity

Package NDC 69367-357-16
Digits Only 6936735716
Product NDC 69367-357
Product ID 69367-357_829b32b5-8c54-455c-83cb-d8dfb7d4407f
Description

473 mL in 1 BOTTLE (69367-357-16)

Marketing

Marketing Status
Marketed Since 2023-10-13
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": "829b32b5-8c54-455c-83cb-d8dfb7d4407f", "openfda": {"unii": ["YQE403BP4D"], "rxcui": ["702519"], "spl_set_id": ["0ca8847d-1966-47a0-995e-a5c0d2fd699d"], "manufacturer_name": ["Westminster Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "473 mL in 1 BOTTLE (69367-357-16)", "package_ndc": "69367-357-16", "marketing_start_date": "20231013"}], "brand_name": "Phenobarbital", "product_id": "69367-357_829b32b5-8c54-455c-83cb-d8dfb7d4407f", "dosage_form": "LIQUID", "product_ndc": "69367-357", "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": "20231013", "listing_expiration_date": "20261231"}