Berberis vulgaris 1X

Product NDC
69152-1552
11-digit product format
691521552
Labeler code
69152
Product ID
69152-1552_1e232c93-4a1a-37c6-e054-00144ff88e88
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Berberis vulgaris
Dosage form
LIQUID
Route
ORAL
Labeler
Paramesh Banerji Life Sciences LLC
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2015-06-04
Marketing end
0000-00-00
Substance
BERBERIS VULGARIS ROOT BARK
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
69152-1552-12020-01-31C16284748780-19d75b9d0-a6d2-f424-e053-dadaa90a57ce17b0b6e9-1805-6488-e054-00144ff88e88

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69152-1552-1Berberis vulgaris 1X8 mL in 1 BOTTLE, DROPPERLIQUID83

DailyMed Socrata Ingredients#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69152-1552BERBERIS VULGARIS 1X (BERBERIS VULGARIS) LIQUID [PARAMESH BANERJI LIFE SCIENCES LLC]3Legacy NDC, 1 package rows20150825_17b0b6e9-1805-6488-e054-00144ff88e88.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsStatus
69152-1552-1691521552018 mL in 1 BOTTLE, DROPPER8 mlHistorical