LACHESIS M

Product NDC
15631-2812
11-digit product format
156312812
Labeler code
15631
Product ID
15631-2812_1a236753-b79c-10f8-e063-6294a90ab3f9
Type
HUMAN OTC DRUG
Nonproprietary name
LACHESIS M
Dosage form
LIQUID
Route
ORAL
Labeler
Rxhomeo Private Limited d.b.a. Rxhomeo, Inc
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2024-05-23
Substance
LACHESIS MUTA VENOM
Active strength
8 [hp_X]/mL
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
LACHESIS M
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
LACHESIS MUTA VENOM8 [hp_X]/mL

Harmonized Identifiers#

Field, Values table
FieldValues
UniiVSW71SS07I

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
15631-2812-0LACHESIS M10 mL in 1 BOTTLELIQUID101
15631-2812-1LACHESIS M30 mL in 1 BOTTLELIQUID301

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
15631-2812LACHESIS M LIQUID [RXHOMEO PRIVATE LIMITED D.B.A. RXHOMEO, INC]1Current NDC, 2 package rows20240606_1a2361f9-226d-0b55-e063-6394a90a083c.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
15631-2812-01563128120010 mL in 1 BOTTLE (15631-2812-0) 10 ml2024-05-23NoNoCurrent
15631-2812-11563128120130 mL in 1 BOTTLE (15631-2812-1) 30 ml2024-05-23NoNoCurrent