Cuprite 3 Special Order

Product NDC
48951-3137
11-digit product format
489513137
Labeler code
48951
Product ID
48951-3137_6aade953-e8cb-765b-e053-2a91aa0a20af
Type
HUMAN OTC DRUG
Nonproprietary name
Cuprite 3 Special Order
Dosage form
POWDER
Route
ORAL
Labeler
Uriel Pharmacy Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2009-09-01
Marketing end
0000-00-00
Substance
CUPRIC OXIDE
Active strength
3 [hp_X]/g
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
0306390c-dd77-4363-afe0-63c58088b2a1Product name120220120
503ea967-4b9c-48cf-9e87-c7975295849dProduct name220220120

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
48951-3137-4Cuprite 3 Special Order60 g in 1 BOTTLE, GLASSPOWDER602

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
CUPRIC OXIDEACTIVE INGREDIENTV1XJQ704R4CUPRITE 3 SPECIAL ORDER POWDER [URIEL PHARMACY INC.]1
CUPRIC CATIONACTIVE MOIETY8CBV67279LCUPRITE 3 SPECIAL ORDER POWDER [URIEL PHARMACY INC.]1
LACTOSEINACTIVE INGREDIENTJ2B2A4N98GCUPRITE 3 SPECIAL ORDER POWDER [URIEL PHARMACY INC.]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48951-3137CUPRITE 3 SPECIAL ORDER POWDER [URIEL PHARMACY INC.]2Legacy NDC, 1 package rows20180425_3b5f133f-f0cb-4e99-8092-eb8822daf7cb.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
48951-3137-44895131370460 g in 1 BOTTLE, GLASS (48951-3137-4) 60 g2009-09-010000-00-00NoNoCurrent