FDA.reportPublic FDA data

Thymuline

Product NDC
71753-1152
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

NDC auxiliary status#

Explicit status records from FDA unfinished, excluded, and compounder auxiliary files. Absence of a row is not itself a regulatory status. Browse every current auxiliary row, including rows without a usable NDC. · Browse every captured source and parsed snapshot.

Current NDC status page 1 of 1 · 2 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded productproduct71753-1152DDiscontinued by firm2026-08-03
excluded packagepackage71753-115271753-1152-1DDiscontinued by firm2026-08-03

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71753-1152THYMULINE LIQUID [RATIS, LLC]2Legacy NDC20220309_8dfaeb98-df5b-4d18-95a8-07f6d7a4cfca.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
71753-1152-17175311520130 mL in 1 BOTTLE, SPRAY (71753-1152-1) 30 ml2018-09-060000-00-00NoNoCurrent