Glandula Thymus 4

Product NDC
48951-5012
11-digit product format
489515012
Labeler code
48951
Product ID
48951-5012_4420d057-a64d-30e3-e063-6394a90a6e5d
Type
HUMAN OTC DRUG
Nonproprietary name
Glandula Thymus 4
Dosage form
LIQUID
Route
ORAL
Labeler
Uriel Pharmacy Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2009-09-01
Substance
BOS TAURUS THYMUS
Active strength
4 [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 Thymus 4
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
BOS TAURUS THYMUS4 [hp_X]/mL

Harmonized Identifiers#

Field, Values table
FieldValues
Unii8XEJ88V2T8

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
48951-5012-1Glandula Thymus 410 in 1 BOXLIQUID106
48951-5012-1Glandula Thymus 41 mL in 1 AMPULELIQUID16

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
BOS TAURUS THYMUSACTIVE INGREDIENT8XEJ88V2T8GLANDULA THYMUS 4 LIQUID [URIEL PHARMACY INC.]1
BOS TAURUS THYMUSACTIVE MOIETY8XEJ88V2T8GLANDULA THYMUS 4 LIQUID [URIEL PHARMACY INC.]1
SODIUM CHLORIDEINACTIVE INGREDIENT451W47IQ8XGLANDULA THYMUS 4 LIQUID [URIEL PHARMACY INC.]1
WATERINACTIVE INGREDIENT059QF0KO0RGLANDULA THYMUS 4 LIQUID [URIEL PHARMACY INC.]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48951-5012GLANDULA THYMUS 4 LIQUID [URIEL PHARMACY INC.]5Current NDC, Legacy NDC, 2 package rows20241108_2fbf59c4-3682-498f-b5c7-6a1122d81058.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
48951-5012-14895150120110 AMPULE in 1 BOX (48951-5012-1) / 1 mL in 1 AMPULE10 ampule2009-09-010000-00-00NoNoCurrent