Allium Cepa

Product NDC
76472-4001
Requested package NDC
76472-4001-1
11-digit product format
764724001
Labeler code
76472
Product ID
76472-4001_e11d5f14-e466-e893-e053-2995a90af3b7
Type
HUMAN OTC DRUG
Nonproprietary name
Allium Cepa
Dosage form
PELLET
Route
SUBLINGUAL
Labeler
SEVENE USA
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2011-11-20
Marketing end
0000-00-00
Substance
ONION
Active strength
200 [kp_C]/1
Pharmacologic classes
Allergens [CS], Cell-mediated Immunity [PE], Dietary Proteins [CS], Increased Histamine Release [PE], Non-Standardized Food Allergenic Extract [EPC], Vegetable Proteins [CS]
NDC exclude flag
No
Listing certified through
2023-12-31
Current FDA listing
Historical FDA.report record

NDC auxiliary status#

Explicit status records from FDA unfinished, excluded, and compounder auxiliary files. Absence of a row is not itself a regulatory status. Browse every current auxiliary row, including rows without a usable NDC. · Browse every captured source and parsed snapshot.

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

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded packagepackage76472-400176472-4001-1DDiscontinued by firm2026-08-03

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
76472-4001-17647240010180 PELLET in 1 CYLINDER (76472-4001-1) 80 pellet2011-11-200000-00-00NoNoCurrent