Bovista 30C

Product NDC
69152-1093
11-digit product format
691521093
Labeler code
69152
Product ID
69152-1093_18c70ca5-56cd-1978-e054-00144ff8d46c
Type
HUMAN OTC DRUG
Nonproprietary name
Bovista
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
LYCOPERDON UTRIFORME FRUITING BODY
Active strength
30 [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
69152-1093-12020-01-31C16284748780-19d75b9d1-269a-f424-e053-dadaa90a57ce18c70ca5-56cc-1978-e054-00144ff8d46c

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69152-1093-1Bovista 30C96 in 1 BOTTLEPELLET961

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69152-1093BOVISTA 30C (BOVISTA) PELLET [PARAMESH BANERJI LIFE SCIENCES LLC]1Legacy NDC, 1 package rows20160427_18c70ca5-56cc-1978-e054-00144ff8d46c.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionStatus
69152-1093-16915210930196 in 1 BOTTLEHistorical