phenobarbital

Generic: phenobarbital

Labeler: hikma pharmaceuticals usa inc.
NDC Directory HUMAN PRESCRIPTION DRUG UNAPPROVED DRUG OTHER Inactive Finished

Drug Facts

Product Profile

Brand Name phenobarbital
Generic Name phenobarbital
Labeler hikma pharmaceuticals usa inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

phenobarbital 60 mg/1

Manufacturer
Hikma Pharmaceuticals USA Inc.

Identifiers & Regulatory

Product NDC 0143-1455
Product ID 0143-1455_3ccf4b4a-2458-4ea0-8feb-8f3ff9980bb5
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category UNAPPROVED DRUG OTHER
DEA Schedule civ
Listing Expiration 2026-12-31
Marketing Start 1999-01-11

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 01431455
Hyphenated Format 0143-1455

Supplemental Identifiers

RxCUI
198083 198089 312357 312362
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
  • 60 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (0143-1455-01)
  • 500 TABLET in 1 BOTTLE (0143-1455-05)
source: ndc

Packages (2)

0143-1455-01 100 TABLET in 1 BOTTLE (0143-1455-01) 0143-1455-05 500 TABLET in 1 BOTTLE (0143-1455-05)

Ingredients (1)

phenobarbital (60 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": "3ccf4b4a-2458-4ea0-8feb-8f3ff9980bb5", "openfda": {"unii": ["YQE403BP4D"], "rxcui": ["198083", "198089", "312357", "312362"], "spl_set_id": ["8f02e85a-6dca-467d-b2bf-ab2f9fa9ef3b"], "manufacturer_name": ["Hikma Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (0143-1455-01)", "package_ndc": "0143-1455-01", "marketing_start_date": "19990111"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (0143-1455-05)", "package_ndc": "0143-1455-05", "marketing_start_date": "19990111"}], "brand_name": "Phenobarbital", "product_id": "0143-1455_3ccf4b4a-2458-4ea0-8feb-8f3ff9980bb5", "dosage_form": "TABLET", "product_ndc": "0143-1455", "dea_schedule": "CIV", "generic_name": "Phenobarbital", "labeler_name": "Hikma Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Phenobarbital", "active_ingredients": [{"name": "PHENOBARBITAL", "strength": "60 mg/1"}], "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "19990111", "listing_expiration_date": "20261231"}