Ustilago maydis 200C

Product NDC
69152-1105
11-digit product format
691521105
Labeler code
69152
Product ID
69152-1105_19152436-8fbc-3412-e054-00144ff8d46c
Type
HUMAN OTC DRUG
Nonproprietary name
Ustilago maydis
Dosage form
PELLET
Route
ORAL
Labeler
Paramesh Banerji Life Sciences LLC
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2015-06-22
Marketing end
0000-00-00
Substance
USTILAGO MAYDIS
Active strength
200 [hp_C]/1
NDC exclude flag
E
Listing certified through
2018-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
69152-1105-12020-01-31C16284748780-19d75b9d0-6001-f424-e053-dadaa90a57ce19152436-8fbb-3412-e054-00144ff8d46c

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69152-1105-1Ustilago maydis 200C96 in 1 BOTTLEPELLET961

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69152-1105USTILAGO MAYDIS 200C (USTILAGO MAYDIS) PELLET [PARAMESH BANERJI LIFE SCIENCES LLC]1Legacy NDC, 1 package rows20170612_19152436-8fbb-3412-e054-00144ff8d46c.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionStatus
69152-1105-16915211050196 in 1 BOTTLEHistorical