Caulophyllum thalictroides 200C

Product NDC
69152-1030
11-digit product format
691521030
Labeler code
69152
Product ID
69152-1030_31b4899f-63c0-24de-e054-00144ff8d46c
Type
HUMAN OTC DRUG
Nonproprietary name
Caulophyllum thalictroides
Dosage form
PELLET
Route
ORAL
Labeler
Paramesh Banerji Life Sciences LLC
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2015-06-17
Marketing end
0000-00-00
Substance
CAULOPHYLLUM THALICTROIDES ROOT
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
69152-1030-12020-01-31C16284748780-19d75b9cf-f3c8-f424-e053-dadaa90a57ce18b49b87-39fe-4b8e-e054-00144ff8d46c

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69152-1030-1Caulophyllum thalictroides 200C96 in 1 BOTTLEPELLET962

DailyMed Socrata Ingredients#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69152-1030CAULOPHYLLUM THALICTROIDES 200C (CAULOPHYLLUM THALICTROIDES) PELLET [PARAMESH BANERJI LIFE SCIENCES LLC]2Legacy NDC, 1 package rows20160504_18b49b87-39fe-4b8e-e054-00144ff8d46c.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionStatus
69152-1030-16915210300196 in 1 BOTTLEHistorical