Home NDC 61727-343-21 Thymuline
Product NDC 61727-343
Requested package NDC 61727-343-21
11-digit product format 617270343
Labeler code 61727
Product ID 61727-343_82fbd741-e798-cd82-e053-2991aa0a7cad
Type HUMAN OTC DRUG
Nonproprietary name NONATHYMULIN
Dosage form PELLET
Route SUBLINGUAL
Labeler Homeocare Laboratories
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2012-11-09
Substance NONATHYMULIN
Active strength 9 [hp_C]/4g
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base Thymuline
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength NONATHYMULIN 9 [hp_C]/4g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 9H198D04WL Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 61727-343-21 Thymuline 4 g in 1 TUBE PELLET 4 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 61727-343 THYMULINE (NONATHYMULIN) PELLET [HOMEOCARE LABORATORIES] 2 Current NDC, Legacy NDC, 1 package rows 20190301_1c3a713d-b6bf-4a3c-b7e2-93a3d80412b3.zip
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 1 of 1 · 1 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 61727-343-21 61727034321 4 g in 1 TUBE (61727-343-21) 4 g 2012-11-09 0000-00-00 No No Current