phenobarbital

Generic: phenobarbital

Labeler: endo usa, inc.
NDC Directory HUMAN PRESCRIPTION DRUG UNAPPROVED DRUG OTHER Inactive Finished

Drug Facts

Product Profile

Brand Name phenobarbital
Generic Name phenobarbital
Labeler endo usa, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

phenobarbital 16.2 mg/1

Manufacturer
Endo USA, Inc.

Identifiers & Regulatory

Product NDC 0603-5165
Product ID 0603-5165_670a5f53-11d3-4132-b6e5-4ad63852cfa7
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category UNAPPROVED DRUG OTHER
DEA Schedule civ
Listing Expiration 2026-12-31
Marketing Start 2002-03-01

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 06035165
Hyphenated Format 0603-5165

Supplemental Identifiers

RxCUI
198086 199164 199167 199168
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
  • 16.2 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE, PLASTIC (0603-5165-21)
  • 1000 TABLET in 1 BOTTLE, PLASTIC (0603-5165-32)
source: ndc

Packages (2)

0603-5165-21 100 TABLET in 1 BOTTLE, PLASTIC (0603-5165-21) 0603-5165-32 1000 TABLET in 1 BOTTLE, PLASTIC (0603-5165-32)

Ingredients (1)

phenobarbital (16.2 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": "670a5f53-11d3-4132-b6e5-4ad63852cfa7", "openfda": {"unii": ["YQE403BP4D"], "rxcui": ["198086", "199164", "199167", "199168"], "spl_set_id": ["069b92ce-0061-4724-8c25-08d8596770a2"], "manufacturer_name": ["Endo USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (0603-5165-21)", "package_ndc": "0603-5165-21", "marketing_start_date": "20020301"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE, PLASTIC (0603-5165-32)", "package_ndc": "0603-5165-32", "marketing_start_date": "20020301"}], "brand_name": "Phenobarbital", "product_id": "0603-5165_670a5f53-11d3-4132-b6e5-4ad63852cfa7", "dosage_form": "TABLET", "product_ndc": "0603-5165", "dea_schedule": "CIV", "generic_name": "phenobarbital", "labeler_name": "Endo USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Phenobarbital", "active_ingredients": [{"name": "PHENOBARBITAL", "strength": "16.2 mg/1"}], "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "20020301", "listing_expiration_date": "20261231"}