Home NDC 51293-694-01 Phenobarbital
Product NDC 51293-694
Requested package NDC 51293-694-01
11-digit product format 512930694
Labeler code 51293
Product ID 51293-694_58537154-b235-b10f-e063-6394a90a9c09
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name phenobarbital
Dosage form TABLET
Route ORAL
Labeler ECI Pharmaceuticals, LLC
Marketing category UNAPPROVED DRUG OTHER
Marketing start 2020-03-01
Substance PHENOBARBITAL
Active strength 100 mg/1
DEA schedule CIV
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes 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 · 15 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Snapshot, Source SHA-256 table Captured / source date Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 f5e01cc5f278…a2eaf40c39c3…2025-04-01 02:39 UTC · source 2025-03-31 2ef7874e63bc…57b86245f4fa…2025-03-28 20:22 UTC · source 2025-03-28 a1b67e2a42f9…c4cf2c586c0d…2025-03-22 03:12 UTC · source 2025-03-21 cfe11265f3b6…090c488252e2…2025-03-10 12:48 UTC · source 2025-03-10 cdf11ea48f46…ba0047e9e063…2025-02-02 03:52 UTC · source 2025-01-31 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 0efc9e666f02…f202fb6c5f17…2024-11-09 02:27 UTC · source 2024-11-08 ad56d346431e…cc804d4bbf1e…2024-10-04 04:10 UTC · source 2024-10-03 367a005e9d99…383a685ebd0f…2024-07-10 04:00 UTC · source 2024-07-09 557ba5c1ecfa…9c80585c8c6e…2024-05-28 21:12 UTC · source 2024-05-28 8af77b9d5b6f…d9bbb34c5368…2024-05-15 03:39 UTC · source 2024-05-14 834df4deac94…adcc014656a3…2024-03-11 06:39 UTC · source 2024-03-08 1332a3947898…d4bfe170f9cd…
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base Phenobarbital
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength PHENOBARBITAL 100 mg/1
DailyMed Product Concepts# FDA-Initiated Inactive NDC Indexing# NDC, Effective, Related label table NDC Effective Related label 51293-694-01 2024-01-30 PHENOBARBITAL TABLETS, USP CIV Rx only 51293-694-05 2024-01-30 PHENOBARBITAL TABLETS, USP CIV Rx only 51293-694-10 2024-01-30 PHENOBARBITAL TABLETS, USP CIV Rx only 51293-694-01 2022-03-03 PHENOBARBITAL TABLETS, USP CIV Rx only 51293-694-05 2022-03-03 PHENOBARBITAL TABLETS, USP CIV Rx only 51293-694-10 2022-03-03 PHENOBARBITAL TABLETS, USP CIV Rx only 51293-694-01 2022-01-28 PHENOBARBITAL TABLETS, USP CIV Rx only 51293-694-05 2022-01-28 PHENOBARBITAL TABLETS, USP CIV Rx only 51293-694-10 2022-01-28 PHENOBARBITAL TABLETS, USP CIV Rx only
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 51293-694 PHENOBARBITAL TABLET [ECI PHARMACEUTICALS, LLC] 7 Current NDC, Legacy NDC 20220304_ac57a37d-79ae-49b4-a5e5-b6f03481a225.zip
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 51293-694-01 51293069401 100 TABLET in 1 BOTTLE, PLASTIC (51293-694-01) 100 tablet 2020-03-01 0000-00-00 No No Current