Albendazole
- Product NDC
- 42291-093
- 11-digit product format
- 422910093
- Labeler code
- 42291
- Product ID
- 42291-093_d5417d66-0add-a04d-e053-2995a90a9d7f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Albendazole
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- AvKARE
- Application
- ANDA210011
- Marketing category
- ANDA
- Marketing start
- 2020-05-15
- Marketing end
- 0000-00-00
- Substance
- ALBENDAZOLE
- Active strength
- 200 mg/1
- Pharmacologic classes
- Anthelmintic [EPC],Cytochrome P450 1A Inducers [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 42291-093-02 | Albendazole200 mg | 2 in 1 BOTTLE | TABLET, FILM COATED | 2 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 42291-093 | ALBENDAZOLE 200 MG (ALBENDAZOLE) TABLET, FILM COATED [AVKARE] | 3 | Legacy NDC, 1 package rows | 20230707_a5b09ffd-6ebe-cd89-e053-2995a90aa281.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 42291-093-02 | 42291009302 | 2 TABLET, FILM COATED in 1 BOTTLE (42291-093-02) | 2020-05-15 | 0000-00-00 | No | No | Current |