Home NDC 76472-1150 Lachesis Mutus
Product NDC 76472-1150
11-digit product format 764721150
Labeler code 76472
Product ID 76472-1150_35b75182-a5fb-1d2d-e063-6394a90ac78d
Type HUMAN OTC DRUG
Nonproprietary name LACHESIS MUTA VENOM
Dosage form PELLET
Route SUBLINGUAL
Labeler SEVENE USA
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2011-11-30
Substance LACHESIS MUTA VENOM
Active strength 30 [hp_C]/1
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base Lachesis Mutus
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength LACHESIS MUTA VENOM 30 [hp_C]/1
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination VSW71SS07I Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 76472-1150-1 Lachesis Mutus 80 in 1 CYLINDER PELLET 80 22
DailyMed Socrata Ingredients# DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 76472-1150 LACHESIS MUTUS (LACHESIS MUTA VENOM) PELLET [SEVENE USA] 22 Current NDC, Legacy NDC, 1 package rows 20250523_cf7139b1-1741-4d03-ab79-559924076682.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 Units Marketing start Marketing end Sample Exclude flag Status 76472-1150-1 76472115001 80 PELLET in 1 CYLINDER (76472-1150-1) 80 pellet 2011-11-30 0000-00-00 No No Current