FDA.reportPublic FDA data

Asterias rubens

Product NDC
71919-096
Requested package NDC
71919-096-08
11-digit product format
719190096
Labeler code
71919
Product ID
71919-096_7e396b4f-5cde-d733-e053-2991aa0aabd6
Type
HUMAN OTC DRUG
Nonproprietary name
ASTERIAS RUBENS
Dosage form
LIQUID
Route
ORAL
Labeler
Washington Homeopathic Products
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2010-06-21
Marketing end
0000-00-00
Substance
ASTERIAS RUBENS
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 packagepackage71919-09671919-096-08DDiscontinued by firm2026-08-03

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
71919-096-087191900960830 mL in 1 VIAL, GLASS (71919-096-08) 30 ml2010-06-210000-00-00NoNoCurrent