phenobarbital

Generic: phenobarbital

Labeler: westminster pharmaceuticals, llc
NDC Directory HUMAN PRESCRIPTION DRUG UNAPPROVED DRUG OTHER Inactive Finished

Drug Facts

Product Profile

Brand Name phenobarbital
Generic Name phenobarbital
Labeler westminster pharmaceuticals, llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

phenobarbital 30 mg/1

Manufacturer
Westminster Pharmaceuticals, LLC

Identifiers & Regulatory

Product NDC 69367-692
Product ID 69367-692_b8256561-2c8d-4b02-8a59-5fbc524e4eb3
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category UNAPPROVED DRUG OTHER
DEA Schedule civ
Listing Expiration 2026-12-31
Marketing Start 2023-09-08

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 69367692
Hyphenated Format 69367-692

Supplemental Identifiers

RxCUI
198083 198089 312357 312362
UPC
0369367692014 0369367693011 0369367694018 0369367691017
UNII
YQE403BP4D

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name phenobarbital (source: ndc)
Generic Name phenobarbital (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 30 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (69367-692-01)
  • 500 TABLET in 1 BOTTLE (69367-692-05)
source: ndc

Packages (2)

69367-692-01 100 TABLET in 1 BOTTLE (69367-692-01) 69367-692-05 500 TABLET in 1 BOTTLE (69367-692-05)

Ingredients (1)

phenobarbital (30 mg/1)

Linked Drug Pages (1)

Phenobarbital ndc-match (0.9)

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 (69367-692-01)", "package_ndc": "69367-692-01", "marketing_start_date": "20230908"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (69367-692-05)", "package_ndc": "69367-692-05", "marketing_start_date": "20230908"}], "brand_name": "Phenobarbital", "product_id": "69367-692_b8256561-2c8d-4b02-8a59-5fbc524e4eb3", "dosage_form": "TABLET", "product_ndc": "69367-692", "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": "30 mg/1"}], "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "20230908", "listing_expiration_date": "20261231"}