Home NDC 0220-1435 Cocculus indicus
Product NDC 0220-1435
11-digit product format 002201435
Labeler code 0220
Product ID 0220-1435_00edbc64-9d35-5751-e063-6294a90a400b
Type HUMAN OTC DRUG
Nonproprietary name ANAMIRTA COCCULUS SEED
Dosage form PELLET
Route ORAL
Labeler Boiron
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 1983-03-03
Substance ANAMIRTA COCCULUS SEED
Active strength 6 [hp_X]/6[hp_X]
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base Cocculus indicus
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ANAMIRTA COCCULUS SEED 6 [hp_X]/6[hp_X]
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 810258W28U Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 0220-1435-41 Cocculus indicus 6 [hp_X] in 1 TUBE PELLET 6 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 0220-1435 COCCULUS INDICUS (ANAMIRTA COCCULUS SEED ) PELLET [BOIRON] 2 Current NDC, Legacy NDC, 1 package rows 20230721_853c0bbd-0b15-5eb0-e053-2991aa0a4c6a.zip
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 1 of 1 · 1 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Marketing start Marketing end Sample Exclude flag Status 0220-1435-41 00220143541 6 [hp_X] in 1 TUBE (0220-1435-41) 1983-03-03 0000-00-00 No No Current