Mandragora 10 Special Order

Product NDC
48951-7140
11-digit product format
489517140
Labeler code
48951
Product ID
48951-7140_006f75dc-e2ff-4b51-b4f3-d5ec56f0221b
Type
HUMAN OTC DRUG
Nonproprietary name
Mandragora 10 Special Order
Dosage form
OINTMENT
Route
TOPICAL
Labeler
Uriel Pharmacy Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2009-09-01
Marketing end
0000-00-00
Substance
MANDRAGORA OFFICINARUM ROOT
Active strength
1 [hp_X]/g
NDC exclude flag
No
Listing certified through
2019-12-31
Current FDA listing
Historical FDA.report record

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
ebc62596-fc97-4d03-9483-7ba095d25db7Product name120151210

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
48951-7140-52020-01-31C16284748780-19d75b9d0-e9f2-f424-e053-dadaa90a57ceMandragora 10 Special Order

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
48951-7140-5Mandragora 10 Special Order60 g in 1 TUBEOINTMENT601

DailyMed Socrata Ingredients#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48951-7140MANDRAGORA 10 SPECIAL ORDER OINTMENT [URIEL PHARMACY INC.]1Legacy NDC, 1 package rows20141217_27d3ee9e-f0cc-48ed-a947-9acc05a537ea.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsStatus
48951-7140-54895171400560 g in 1 TUBE60 gHistorical