Rauwolfia serpentina 1X

Product NDC
69152-1559
11-digit product format
691521559
Labeler code
69152
Product ID
69152-1559_16fac81e-d49d-5fdd-e054-00144ff88e88
Type
HUMAN OTC DRUG
Nonproprietary name
Rauwolfia serpentina
Dosage form
LIQUID
Route
ORAL
Labeler
Paramesh Banerji Life Sciences LLC
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2015-05-26
Marketing end
0000-00-00
Substance
RAUWOLFIA SERPENTINA
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
69152-1559-12020-01-31C16284748780-19d75b9cf-ee16-f424-e053-dadaa90a57ce16fac81e-d49c-5fdd-e054-00144ff88e88

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69152-1559-1Rauwolfia serpentina 1X8 mL in 1 BOTTLE, DROPPERLIQUID81

DailyMed Socrata Ingredients#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69152-1559RAUWOLFIA SERPENTINA 1X (RAUWOLFIA SERPENTINA) LIQUID [PARAMESH BANERJI LIFE SCIENCES LLC]1Legacy NDC, 1 package rows20150527_16fac81e-d49c-5fdd-e054-00144ff88e88.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsStatus
69152-1559-1691521559018 mL in 1 BOTTLE, DROPPER8 mlHistorical