Home NDC 71753-1152-1 Thymuline
Product NDC 71753-1152
Requested package NDC 71753-1152-1
11-digit product format 717531152
Labeler code 71753
Product ID 71753-1152_ff94c869-5b3e-43a2-8935-9372fb2333fa
Type HUMAN OTC DRUG
Nonproprietary name Thymuline
Dosage form LIQUID
Route ORAL
Labeler Ratis, LLC
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2018-09-06
Marketing end 2025-12-01
Substance NONATHYMULIN
Active strength 9 [hp_C]/mL
NDC exclude flag No
Listing certified through 0000-00-00
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 71753-1152 71753-1152-1 D Discontinued by firm excluded / ndc_excluded.zip d630ba8d3edf…732f749b63fb…
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 71753-1152 THYMULINE LIQUID [RATIS, LLC] 2 Legacy NDC 20220309_8dfaeb98-df5b-4d18-95a8-07f6d7a4cfca.zip
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 71753-1152-1 71753115201 30 mL in 1 BOTTLE, SPRAY (71753-1152-1) 30 ml 2018-09-06 2025-12-01 No No Current