Lachesis
- Product NDC
- 44911-0388
- 11-digit product format
- 449110388
- Labeler code
- 44911
- Product ID
- 44911-0388_1bf41e20-8205-44f4-a88a-851b6c708db3
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Lachesis Mutus
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Energique, Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2016-08-22
- Substance
- LACHESIS MUTA VENOM
- Active strength
- 200 [hp_C]/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
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| LACHESIS MUTA VENOM | 200 [hp_C]/mL |
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 |
|---|
| 44911-0388-1 | Lachesis | 30 mL in 1 BOTTLE, DROPPER | LIQUID | 30 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 44911-0388 | LACHESIS (LACHESIS MUTUS) LIQUID [ENERGIQUE, INC.] | 4 | Current NDC, Legacy NDC, 1 package rows | 20241030_25c87c59-6b32-494e-8c10-b34fa8bbd53d.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 44911-0388-1 | 44911038801 | 30 mL in 1 BOTTLE, DROPPER (44911-0388-1) | 30 ml | 2016-08-22 | 0000-00-00 | No | No | Current |