Helleborus Berberis Special Order

Product NDC
48951-5036
11-digit product format
489515036
Labeler code
48951
Product ID
48951-5036_6dd63c1f-e59f-e73f-e053-2a91aa0af677
Type
HUMAN OTC DRUG
Nonproprietary name
Helleborus Berberis Special Order
Dosage form
PELLET
Route
ORAL
Labeler
Uriel Pharmacy Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2009-09-01
Marketing end
0000-00-00
Substance
ARISTOLOCHIA CLEMATITIS WHOLE; HELLEBORUS FOETIDUS ROOT; POTASSIUM ALUM; BERBERIS VULGARIS ROOT BARK
Active strength
3 [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1
NDC exclude flag
No
Listing certified through
2020-12-31
Current FDA listing
Historical FDA.report record

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 2 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded productproduct48951-5036IInactivated by FDA2026-08-17
excluded packagepackage48951-503648951-5036-2IInactivated by FDA2026-08-17

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
48951-5036-2Helleborus Berberis Special Order1350 in 1 BOTTLE, GLASSPELLET13501

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48951-5036HELLEBORUS BERBERIS SPECIAL ORDER PELLET [URIEL PHARMACY INC.]1Legacy NDC, 1 package rows20180605_6dd63c1f-e59e-e73f-e053-2a91aa0af677.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
48951-5036-2489515036021350 PELLET in 1 BOTTLE, GLASS (48951-5036-2) 1350 pellet2009-09-010000-00-00NoNoCurrent