Angelica sinensis, radix

Product NDC
71919-058
11-digit product format
719190058
Labeler code
71919
Product ID
71919-058_7e3a5d34-a8b9-06e6-e053-2991aa0aa850
Type
HUMAN OTC DRUG
Nonproprietary name
ANGELICA SINENSIS ROOT
Dosage form
LIQUID
Route
ORAL
Labeler
Washington Homeopathic Products
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2015-06-12
Marketing end
0000-00-00
Substance
ANGELICA SINENSIS ROOT
Active strength
30 [hp_C]/mL
NDC exclude flag
No
Listing certified through
2019-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#