Crotoxin
- Product NDC
- 48142-400
- 11-digit product format
- 481420400
- Labeler code
- 48142
- Product ID
- 48142-400_8ac1e6de-a534-4abd-8067-b90ce952e8fe
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- crotalus durissus terrificus venom
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAVENOUS
- Labeler
- Celtic Biotech Iowa, Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2018-04-30
- Marketing end
- 0000-00-00
- Substance
- CROTALUS DURISSUS TERRIFICUS VENOM
- Active strength
- 4 [hp_X]/mL
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 48142-400-40 | Crotoxin | 10 mL in 1 VIAL, MULTI-DOSE | INJECTION, SOLUTION | 10 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 48142-400 | CROTOXIN (CROTALUS DURISSUS TERRIFICUS VENOM) INJECTION, SOLUTION [CELTIC BIOTECH IOWA, INC.] | 1 | Legacy NDC, 1 package rows | 20180430_148af88b-e23c-4493-9b7f-35d993c32d32.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 48142-400-40 | 48142040040 | 10 mL in 1 VIAL, MULTI-DOSE | 10 ml | Historical |