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
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| F4216019LN | ALBENDAZOLE | 54965-21-8 | ALBENDAZOLE |
Packages
| 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 | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Albendazole | Bryant Ranch Prepack | 2024-06-28 | HUMAN PRESCRIPTION DRUG LABEL | 100 |