Hypericum perforatum 200C

Product NDC
69152-1009
11-digit product format
691521009
Labeler code
69152
Product ID
69152-1009_318c79d9-f6d7-7365-e054-00144ff88e88
Type
HUMAN OTC DRUG
Nonproprietary name
Hypericum perforatum
Dosage form
PELLET
Route
ORAL
Labeler
Paramesh Banerji Life Sciences LLC
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2015-05-12
Marketing end
0000-00-00
Substance
HYPERICUM PERFORATUM
Active strength
200 [hp_C]/1
NDC exclude flag
E
Listing certified through
2017-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
69152-1009-12020-01-31C16284748780-19d75b9d0-fb92-f424-e053-dadaa90a57ce15e0d725-022e-0766-e054-00144ff88e88

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69152-1009-1Hypericum perforatum 200C96 in 1 BOTTLEPELLET967

DailyMed Socrata Ingredients#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69152-1009HYPERICUM PERFORATUM 200C (HYPERICUM PERFORATUM) PELLET [PARAMESH BANERJI LIFE SCIENCES LLC]7Legacy NDC, 1 package rows20160428_15e0d725-022e-0766-e054-00144ff88e88.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionStatus
69152-1009-16915210090196 in 1 BOTTLEHistorical