Home NDC 70518-3469 Phenobarbital
Product NDC 70518-3469
11-digit product format 705183469
Labeler code 70518
Product ID 70518-3469_f05a520a-dce3-ee99-e053-2a95a90a4a97
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name Phenobarbital
Dosage form TABLET
Route ORAL
Labeler REMEDYREPACK INC.
Marketing category UNAPPROVED DRUG OTHER
Marketing start 2022-08-09
Marketing end 0000-00-00
Substance PHENOBARBITAL
Active strength 65 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 · 2 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 product product 70518-3469 D Discontinued by firm excluded / ndc_excluded.zip d630ba8d3edf…732f749b63fb…2025-12-14 17:58 UTC · source 2025-12-05 excluded package package 70518-3469 70518-3469-0 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 Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 70518-3469 PHENOBARBITAL TABLET [REMEDYREPACK INC.] 3 Legacy NDC 20240113_ad81fdec-af95-4188-8c7e-cd24d598a05e.zip
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 70518-3469-0 70518346900 30 TABLET in 1 BLISTER PACK (70518-3469-0) 30 tablet 2022-08-09 0000-00-00 No No Current