Package 13517-207-16

Brand: phenobarbital

Generic: phenobarbital
NDC Package

Package Facts

Identity

Package NDC 13517-207-16
Digits Only 1351720716
Product NDC 13517-207
Description

473 mL in 1 BOTTLE, PLASTIC (13517-207-16)

Marketing

Marketing Status
Discontinued 2026-06-30
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": "6ff75bc8-70b3-4ffb-acf9-49a5c3c3dc48", "openfda": {"upc": ["0313517207160"], "unii": ["YQE403BP4D"], "rxcui": ["702519"], "spl_set_id": ["120a0542-7fd8-429e-aada-a936cc65b1f8"], "manufacturer_name": ["e5 Pharma, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "473 mL in 1 BOTTLE, PLASTIC (13517-207-16)", "package_ndc": "13517-207-16", "marketing_end_date": "20260630", "marketing_start_date": "20231103"}], "brand_name": "Phenobarbital", "product_id": "13517-207_6ff75bc8-70b3-4ffb-acf9-49a5c3c3dc48", "dosage_form": "ELIXIR", "product_ndc": "13517-207", "dea_schedule": "CIV", "generic_name": "phenobarbital", "labeler_name": "e5 Pharma, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Phenobarbital", "active_ingredients": [{"name": "PHENOBARBITAL", "strength": "20 mg/5mL"}], "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_end_date": "20260630", "marketing_start_date": "20231103"}