FDA.reportPublic FDA data

Carduus benedictus

Product NDC
71919-165
Requested package NDC
71919-165-09
11-digit product format
719190165
Labeler code
71919
Product ID
71919-165_7e45e32d-7a33-d740-e053-2a91aa0a8775
Type
HUMAN OTC DRUG
Nonproprietary name
CENTAUREA BENEDICTA
Dosage form
LIQUID
Route
ORAL
Labeler
Washington Homeopathic Products
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2012-11-21
Marketing end
0000-00-00
Substance
CENTAUREA BENEDICTA
Active strength
30 [hp_C]/mL
NDC exclude flag
No
Listing certified through
2020-12-31
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 packagepackage71919-16571919-165-09DDiscontinued by firm2026-07-31

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
71919-165-097191901650950 mL in 1 BOTTLE, GLASS (71919-165-09) 50 ml2012-11-210000-00-00NoNoCurrent