Home NDC 81033-164 Phenobarbital Oral Solution
Product NDC 81033-164
11-digit product format 810330164
Labeler code 81033
Product ID 81033-164_446d8928-62fe-1d8e-e063-6394a90a2fe2
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name Phenobarbital Oral
Dosage form SOLUTION
Route ORAL
Labeler Kesin Pharma Corporation
Marketing category UNAPPROVED DRUG OTHER
Marketing start 2025-11-05
Substance PHENOBARBITAL
Active strength 20 mg/5mL
DEA schedule CIV
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base Phenobarbital Oral Solution
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength PHENOBARBITAL 20 mg/5mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination YQE403BP4D Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 702519 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 81033-164-47 Phenobarbital Oral Solution 473 mL in 1 BOTTLE, PLASTIC SOLUTION 473 1
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 1 of 1 · 1 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 81033-164-47 81033016447 473 mL in 1 BOTTLE, PLASTIC (81033-164-47) 473 ml 2025-11-05 No No Current