Home NDC 43063-953-30 Phenobarbital
Product NDC 43063-953
Requested package NDC 43063-953-30
11-digit product format 430630953
Labeler code 43063
Product ID 43063-953_e6db88e4-fc21-090f-e053-2a95a90af0ff
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name phenobarbital
Dosage form TABLET
Route ORAL
Labeler PD-Rx Pharmaceuticals, Inc.
Marketing category UNAPPROVED DRUG OTHER
Marketing start 2017-02-24
Marketing end 0000-00-00
Substance PHENOBARBITAL
Active strength 32 mg/1
DEA schedule CIV
NDC exclude flag No
Listing certified through 2023-12-31
Current FDA listing Historical FDA.report record Observed NDC auxiliary status history# This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
Historic NDC status page 1 of 1 · 1 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Product NDC Package NDC Code Status Reporting period Archive Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 excluded package package 43063-953 43063-953-30 D Discontinued by firm excluded / ndc_excluded.zip d630ba8d3edf…732f749b63fb…
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
DailyMed Product Concepts# DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 43063-953 PHENOBARBITAL TABLET [PD-RX PHARMACEUTICALS, INC.] 12 Legacy NDC 20241018_5d567cef-2480-416b-b4e4-a2e3cb205e9a.zip
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 43063-953-30 43063095330 30 TABLET in 1 BOTTLE, PLASTIC (43063-953-30) 30 tablet 2019-03-06 0000-00-00 No No Current