Eupatorium perfoliatum 1X

Product NDC
69152-1550
11-digit product format
691521550
Labeler code
69152
Product ID
69152-1550_4a4de8b6-d3d1-1a1e-e054-00144ff8d46c
Type
HUMAN OTC DRUG
Nonproprietary name
Eupatorium perfoliatum
Dosage form
LIQUID
Route
ORAL
Labeler
Paramesh Banerji Life Sciences LLC
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2015-04-01
Marketing end
0000-00-00
Substance
EUPATORIUM PERFOLIATUM FLOWERING TOP
Active strength
1 [hp_X]/8mL
NDC exclude flag
E
Listing certified through
2018-12-31
Current FDA listing
Historical FDA.report record

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
7792dadb-52b6-46b6-8fdf-80b1171065b5Product name120180810

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
69152-1550-12020-01-31C16284748780-19d75b9d0-55b1-f424-e053-dadaa90a57ce0a7e3b33-4559-0814-e054-00144ff88e88

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69152-1550-1Eupatorium perfoliatum 1X8 mL in 1 BOTTLE, DROPPERLIQUID84

DailyMed Socrata Ingredients#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69152-1550EUPATORIUM PERFOLIATUM 1X (EUPATORIUM PERFOLIATUM) LIQUID [PARAMESH BANERJI LIFE SCIENCES LLC]4Legacy NDC, 1 package rows20170309_0a7e3b33-4559-0814-e054-00144ff88e88.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsStatus
69152-1550-1691521550018 mL in 1 BOTTLE, DROPPER8 mlHistorical