Baptisia tinctoria 1X

Product NDC
69152-1560
11-digit product format
691521560
Labeler code
69152
Product ID
69152-1560_1e232c93-4a17-37c6-e054-00144ff88e88
Type
HUMAN OTC DRUG
Nonproprietary name
Baptisia tinctoria
Dosage form
LIQUID
Route
ORAL
Labeler
Paramesh Banerji Life Sciences LLC
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2015-05-09
Marketing end
0000-00-00
Substance
BAPTISIA TINCTORIA ROOT
Active strength
1 [hp_X]/8mL
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
69152-1560-12020-01-31C16284748780-19d75b9d0-a6cf-f424-e053-dadaa90a57ce15a4d71a-e312-6395-e054-00144ff88e88

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69152-1560-1Baptisia tinctoria 1X8 mL in 1 BOTTLE, DROPPERLIQUID83

DailyMed Socrata Ingredients#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69152-1560BAPTISIA TINCTORIA 1X (BAPTISIA TINCTORIA) LIQUID [PARAMESH BANERJI LIFE SCIENCES LLC]3Legacy NDC, 1 package rows20150825_15a4d71a-e312-6395-e054-00144ff88e88.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsStatus
69152-1560-1691521560018 mL in 1 BOTTLE, DROPPER8 mlHistorical