Albendazole
- Product NDC
- 72162-2359
- 11-digit product format
- 721622359
- Labeler code
- 72162
- Product ID
- 72162-2359_875c188d-cbe0-410c-89c3-3e97a79c2d12
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Albendazole
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA213435
- Marketing category
- ANDA
- Marketing start
- 2021-02-24
- Substance
- ALBENDAZOLE
- Active strength
- 200 mg/1
- Pharmacologic classes
- Anthelmintic [EPC], Cytochrome P450 1A Inducers [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Albendazole
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ALBENDAZOLE | 200 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | F4216019LN |
| Rxcui | 199672 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 72162-2359-2 | Albendazole | 2 in 1 BOTTLE | TABLET | 2 | | 100 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72162-2359 | ALBENDAZOLE TABLET [BRYANT RANCH PREPACK] | 100 | Current NDC, 1 package rows | 20240702_74aeb307-b408-47b1-bd8f-fe7eeb844466.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 72162-2359-2 | 72162235902 | 2 TABLET in 1 BOTTLE (72162-2359-2) | 2 tablet | 2024-06-28 | No | No | Current |