Package 13517-692-01

Brand: phenobarbital

Generic: phenobarbital
NDC Package

Package Facts

Identity

Package NDC 13517-692-01
Digits Only 1351769201
Product NDC 13517-692
Description

100 TABLET in 1 BOTTLE, PLASTIC (13517-692-01)

Marketing

Marketing Status
Discontinued 2026-11-30
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": "8d7c438d-0331-441f-848f-b832658a8728", "openfda": {"upc": ["0313517693017", "0313517694014", "0313517691013", "0313517692010"], "unii": ["YQE403BP4D"], "rxcui": ["198083", "198089", "312357", "312362"], "spl_set_id": ["5c4efd5a-75be-480b-ac31-40dd66feada1"], "manufacturer_name": ["e5 Pharma, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (13517-692-01)", "package_ndc": "13517-692-01", "marketing_end_date": "20261130", "marketing_start_date": "20221130"}], "brand_name": "Phenobarbital", "product_id": "13517-692_8d7c438d-0331-441f-848f-b832658a8728", "dosage_form": "TABLET", "product_ndc": "13517-692", "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": "30 mg/1"}], "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_end_date": "20261130", "marketing_start_date": "20221130"}