FDA.reportPublic FDA data

TARTARICUM ACIDUM

Product NDC
71919-667
Requested package NDC
71919-667-09
11-digit product format
719190667
Labeler code
71919
Product ID
71919-667_99c0aa0a-d5f1-e8be-e053-2995a90a8f4a
Type
HUMAN OTC DRUG
Nonproprietary name
Tartaric acid
Dosage form
LIQUID
Route
ORAL
Labeler
Washington Homeopathic Products
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2011-05-17
Marketing end
0000-00-00
Substance
TARTARIC ACID
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 packagepackage71919-66771919-667-09DDiscontinued by firm2026-07-31

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
71919-667-097191906670950 mL in 1 BOTTLE, GLASS (71919-667-09) 50 ml2011-05-170000-00-00NoNoCurrent