Home NDC 48951-5144 Glandula thyreoidea 8X
Product NDC 48951-5144
11-digit product format 489515144
Labeler code 48951
Product ID 48951-5144_2ad43b09-30dd-b7cb-e063-6394a90ac6d5
Type HUMAN OTC DRUG
Nonproprietary name Glandula thyreoidea 8X
Dosage form LIQUID
Route ORAL
Labeler Uriel Pharmacy, Inc
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2009-09-01
Substance ORYCTOLAGUS CUNICULUS LIVER
Active strength 8 [hp_X]/mL
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base Glandula thyreoidea 8X
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ORYCTOLAGUS CUNICULUS LIVER 8 [hp_X]/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 7A99K6361Z 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 48951-5144-3 Glandula thyreoidea 8X 60 mL in 1 BOTTLE, DROPPER LIQUID 60 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 48951-5144 GLANDULA THYREOIDEA 8X LIQUID [URIEL PHARMACY, INC] 1 Current NDC, 1 package rows 20250105_2ad43b09-30dc-b7cb-e063-6394a90ac6d5.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 Sample Exclude flag Status 48951-5144-3 48951514403 60 mL in 1 BOTTLE, DROPPER (48951-5144-3) 60 ml 2009-09-01 No No Current