Anacardium orientale 200C

Product NDC
69152-1092
11-digit product format
691521092
Labeler code
69152
Product ID
69152-1092_319d2af1-96ff-3de8-e054-00144ff8d46c
Type
HUMAN OTC DRUG
Nonproprietary name
Anacardium orientale
Dosage form
PELLET
Route
ORAL
Labeler
Paramesh Banerji Life Sciences LLC
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2015-06-18
Marketing end
0000-00-00
Substance
SEMECARPUS ANACARDIUM JUICE
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
69152-1092-12020-01-31C16284748780-19d75b9d0-fbb0-f424-e053-dadaa90a57ce18c6f731-d4a2-09e0-e054-00144ff8d46c

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69152-1092-1Anacardium orientale 200C96 in 1 BOTTLEPELLET962

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69152-1092ANACARDIUM ORIENTALE 200C (ANACARDIUM ORIENTALE) PELLET [PARAMESH BANERJI LIFE SCIENCES LLC]2Legacy NDC, 1 package rows20160429_18c6f731-d4a2-09e0-e054-00144ff8d46c.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionStatus
69152-1092-16915210920196 in 1 BOTTLEHistorical