Ptelea trifoliata

Product NDC
71919-560
11-digit product format
719190560
Labeler code
71919
Product ID
71919-560_7e5abe5e-f7c2-6c38-e053-2a91aa0aa9b4
Type
HUMAN OTC DRUG
Nonproprietary name
PTELEA TRIFOLIATA BARK
Dosage form
LIQUID
Route
ORAL
Labeler
Washington Homeopathic Products
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2009-09-29
Marketing end
0000-00-00
Substance
PTELEA TRIFOLIATA BARK
Active strength
30 [hp_C]/mL
NDC exclude flag
No
Listing certified through
2020-12-31
Current FDA listing
Historical FDA.report record

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
71919-560-077191905600715 mL in 1 VIAL, GLASS (71919-560-07) 15 ml2009-09-290000-00-00NoNoCurrent
71919-560-087191905600830 mL in 1 VIAL, GLASS (71919-560-08) 30 ml2009-09-290000-00-00NoNoCurrent
71919-560-097191905600950 mL in 1 BOTTLE, GLASS (71919-560-09) 50 ml2009-09-290000-00-00NoNoCurrent
71919-560-1071919056010100 mL in 1 BOTTLE, GLASS (71919-560-10) 100 ml2009-09-290000-00-00NoNoCurrent