Bryonia alba 200C

Product NDC
69152-1021
11-digit product format
691521021
Labeler code
69152
Product ID
69152-1021_3be5e6ce-fddf-4e58-e054-00144ff88e88
Type
HUMAN OTC DRUG
Nonproprietary name
Bryonia alba
Dosage form
PELLET
Route
ORAL
Labeler
Paramesh Banerji Life Sciences LLC
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2015-06-02
Marketing end
0000-00-00
Substance
BRYONIA ALBA 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
69152-1021-12020-01-31C16284748780-19d75b9d0-a4b3-f424-e053-dadaa90a57ce178498aa-fb66-6438-e054-00144ff8d46c

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69152-1021-1Bryonia alba 200C96 in 1 BOTTLEPELLET966

DailyMed Socrata Ingredients#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69152-1021BRYONIA ALBA 200C (BRYONIA ALBA) PELLET [PARAMESH BANERJI LIFE SCIENCES LLC]6Legacy NDC, 1 package rows20160907_178498aa-fb66-6438-e054-00144ff8d46c.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionStatus
69152-1021-16915210210196 in 1 BOTTLEHistorical