LACHESIS MUTUS
- Product NDC
- 76472-3022
- 11-digit product format
- 764723022
- Labeler code
- 76472
- Product ID
- 76472-3022_35b7588a-3001-1ce7-e063-6394a90ab714
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- LACHESIS MUTUS
- Dosage form
- PELLET
- Route
- SUBLINGUAL
- Labeler
- SEVENE USA
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2011-11-23
- Substance
- LACHESIS MUTA VENOM
- Active strength
- 200 [kp_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
- Brand name suffix
- 200ck
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| LACHESIS MUTA VENOM | 200 [kp_C]/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | VSW71SS07I |
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 76472-3022-1 | LACHESIS MUTUS200ck | 80 in 1 CYLINDER | PELLET | 80 | | 5 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 76472-3022 | LACHESIS MUTUS 200CK (LACHESIS MUTUS) PELLET [SEVENE USA] | 5 | Current NDC, Legacy NDC, 1 package rows | 20250523_cf85728d-07c8-5a23-e053-2995a90aa6cd.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 76472-3022-1 | 76472302201 | 80 PELLET in 1 CYLINDER (76472-3022-1) | 80 pellet | 2011-11-23 | 0000-00-00 | No | No | Current |