Cortisonum 30 Special Order

Product NDC
48951-3133
11-digit product format
489513133
Labeler code
48951
Product ID
48951-3133_6ccdb407-2c23-7ccc-e053-2991aa0a5eec
Type
HUMAN OTC DRUG
Nonproprietary name
Cortisonum 30 Special Order
Dosage form
LIQUID
Route
ORAL
Labeler
Uriel Pharmacy Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2009-09-01
Marketing end
0000-00-00
Substance
CORTISONE
Active strength
30 [hp_X]/mL
NDC exclude flag
No
Listing certified through
2020-12-31
Current FDA listing
Historical FDA.report record

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
9bfd9c37-f773-6e9a-5f6b-6f5701d62adcProduct name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
48951-3133-1Cortisonum 30 Special Order10 in 1 BOXLIQUID102
48951-3133-1Cortisonum 30 Special Order1 mL in 1 AMPULELIQUID12

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
CORTISONEACTIVE INGREDIENTV27W9254FZCORTISONUM 30 SPECIAL ORDER LIQUID [URIEL PHARMACY INC.]1
CORTISONEACTIVE MOIETYV27W9254FZCORTISONUM 30 SPECIAL ORDER LIQUID [URIEL PHARMACY INC.]1
SODIUM CHLORIDEINACTIVE INGREDIENT451W47IQ8XCORTISONUM 30 SPECIAL ORDER LIQUID [URIEL PHARMACY INC.]1
WATERINACTIVE INGREDIENT059QF0KO0RCORTISONUM 30 SPECIAL ORDER LIQUID [URIEL PHARMACY INC.]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48951-3133CORTISONUM 30 SPECIAL ORDER LIQUID [URIEL PHARMACY INC.]2Legacy NDC, 2 package rows20180522_dd45c189-1e18-40f9-baf0-dbf4c38ddde0.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
48951-3133-14895131330110 AMPULE in 1 BOX (48951-3133-1) > 1 mL in 1 AMPULE10 ampule2009-09-010000-00-00NoNoCurrent