FDA.reportPublic FDA data

Quillaja saponaria

Product NDC
71919-570
11-digit product format
719190570
Labeler code
71919
Product ID
71919-570_7e5af95f-c0ac-d4e4-e053-2a91aa0af3d7
Type
HUMAN OTC DRUG
Nonproprietary name
QUILLAJA SAPONARIA BARK
Dosage form
LIQUID
Route
ORAL
Labeler
Washington Homeopathic Products
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2009-07-31
Marketing end
0000-00-00
Substance
QUILLAJA SAPONARIA BARK
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 · 5 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded productproduct71919-570DDiscontinued by firm2026-07-31
excluded packagepackage71919-57071919-570-07DDiscontinued by firm2026-07-31
excluded packagepackage71919-57071919-570-08DDiscontinued by firm2026-07-31
excluded packagepackage71919-57071919-570-09DDiscontinued by firm2026-07-31
excluded packagepackage71919-57071919-570-10DDiscontinued by firm2026-07-31

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
71919-570-077191905700715 mL in 1 VIAL, GLASS (71919-570-07) 15 ml2009-07-310000-00-00NoNoCurrent
71919-570-087191905700830 mL in 1 VIAL, GLASS (71919-570-08) 30 ml2009-07-310000-00-00NoNoCurrent
71919-570-097191905700950 mL in 1 BOTTLE, GLASS (71919-570-09) 50 ml2009-07-310000-00-00NoNoCurrent
71919-570-1071919057010100 mL in 1 BOTTLE, GLASS (71919-570-10) 100 ml2009-07-310000-00-00NoNoCurrent