Fenbendazole
- Manufacturer
- Spectrum Laboratory Products, Inc.
- Effective date
- 2021-01-26
- Label type
- BULK INGREDIENT
- Version
- 4
- Source
- full-release
- Hydrated at
- 2026-06-01 02:49:52
Label at a glance#
ProductFenbendazole
Active ingredientFENBENDAZOLE
Label structure1 sections
Label contents#
Full prescribing information#
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 49452-3035-1 | Fenbendazole | 5 g in 1 BOTTLE, GLASS | POWDER | 5 | 4 | |
| 49452-3035-2 | Fenbendazole | 25 g in 1 BOTTLE, GLASS | POWDER | 25 | 4 | |
| 49452-3035-3 | Fenbendazole | 100 g in 1 BOTTLE, GLASS | POWDER | 100 | 4 | |
| 49452-3035-4 | Fenbendazole | 1000 g in 1 BOTTLE, GLASS | POWDER | 1000 | 4 | |
| 49452-3035-5 | Fenbendazole | 25000 g in 1 DRUM | POWDER | 25000 | 4 | |
| 49452-3035-6 | Fenbendazole | 5000 g in 1 PAIL | POWDER | 5000 | 4 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 49452-3035 | FENBENDAZOLE POWDER [SPECTRUM LABORATORY PRODUCTS, INC.] | 4 | 6 package rows | 20210128_c4f6cd48-d024-42d1-9932-c5b64be41dd7.zip |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 49452-3035-1 | GM - Gram | 49452-3035 | ea260a61-2e18-438b-a092-10046049b0d6 | 1 | 2017-08-11 |
| 49452-3035-2 | GM - Gram | 49452-3035 | daff0466-9946-4990-b00d-06a20e07bceb | 1 | 2017-08-11 |
| 49452-3035-3 | GM - Gram | 49452-3035 | 4d5d86b0-f875-4b2a-a68e-456e92449e8f | 1 | 2017-08-11 |
| 49452-3035-4 | GM - Gram | 49452-3035 | e91f75a4-e00d-48d8-ad9c-e3dd432d442a | 1 | 2017-08-11 |
| 49452-3035-5 | GM - Gram | 49452-3035 | 6cd2b2be-0e59-4748-b651-cb620e8706fe | 1 | 2017-08-11 |
Products#
Every source-derived product name is available through these pages.
- Fenbendazole
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 49452-3035 | 49452-3035-1, 49452-3035-2, 49452-3035-3, 49452-3035-4, 49452-3035-5, 49452-3035-6 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| FENBENDAZOLE | 621BVT9M36 | ACTIB |
Source Document#
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
