Coumarin

Product NDC
57520-1001
11-digit product format
575201001
Labeler code
57520
Product ID
57520-1001_62eb7062-f7de-4da2-858b-1fb3408709b6
Type
HUMAN OTC DRUG
Nonproprietary name
Coumarinum,
Dosage form
LIQUID
Route
ORAL
Labeler
Apotheca Company
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2011-12-15
Marketing end
2022-11-30
Substance
COUMARIN
Active strength
6 [hp_X]/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
57520-1001-12022-11-14C16284748780-19d75b9d0-dc27-f424-e053-dadaa90a57ce638f5a02-0f10-4cbc-87f8-5b5d4fef209b
57520-1001-12020-01-31C16284748780-19d75b9d0-dc27-f424-e053-dadaa90a57ce638f5a02-0f10-4cbc-87f8-5b5d4fef209b

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
57520-1001-15752010010130 mL in 1 BOTTLE, DROPPER (57520-1001-1) 30 ml2011-12-152022-11-30NoNoCurrent