LACHESIS MUTUS
- Product NDC
- 10191-1459
- 11-digit product format
- 101911459
- Labeler code
- 10191
- Product ID
- 10191-1459_b37faf2d-22b7-4196-a794-0c33cf226a6e
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- BUSHMASTER VENOM
- Dosage form
- PELLET
- Route
- SUBLINGUAL
- Labeler
- REMEDY MAKERS
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2003-05-05
- Marketing end
- 0000-00-00
- Substance
- LACHESIS MUTA VENOM
- Active strength
- 12 [hp_C]/1
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 10191-1459-2 | LACHESIS MUTUS | 147 in 1 VIAL, GLASS | PELLET | 147 | | 1 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 10191-1459 | LACHESIS MUTUS (BUSHMASTER VENOM) PELLET [REMEDY MAKERS] | 1 | Legacy NDC, 1 package rows | 20111102_013689ea-62e1-498a-a53e-fed7767e451e.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 10191-1459-2 | 10191145902 | 147 in 1 VIAL, GLASS | Historical |