Bio Gentian

Product NDC
57520-0461
11-digit product format
575200461
Labeler code
57520
Product ID
57520-0461_5c08ef26-5f5b-4fb9-8b3b-34e19ea12def
Type
HUMAN OTC DRUG
Nonproprietary name
Gentian,
Dosage form
LIQUID
Route
ORAL
Labeler
Apotheca Company
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2010-06-03
Marketing end
2022-09-07
Substance
GENTIANA LUTEA ROOT
Active strength
200 [hp_C]/mL
NDC exclude flag
No
Listing certified through
0000-00-00
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
57520-0461-12022-07-13C16284748780-19d75b9d0-e09b-f424-e053-dadaa90a57cedffdc098-05bd-44aa-a6ff-660fea3887a4
57520-0461-12020-01-31C16284748780-19d75b9d0-e09b-f424-e053-dadaa90a57cedffdc098-05bd-44aa-a6ff-660fea3887a4

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
57520-0461-15752004610130 mL in 1 BOTTLE, DROPPER (57520-0461-1) 30 ml2010-06-032022-09-07NoNoCurrent