Albendazole
- Product NDC
- 63629-1221
- 11-digit product format
- 636291221
- Labeler code
- 63629
- Product ID
- 63629-1221_edc7bf96-bf48-4ea2-8ed6-e060d368eb95
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Albendazole
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA210011
- Marketing category
- ANDA
- Marketing start
- 2018-12-15
- 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 Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 63629-1221 | ALBENDAZOLE 200 MG (ALBENDAZOLE) TABLET, FILM COATED [BRYANT RANCH PREPACK] | 107 | Legacy NDC | 20240814_62aa5d76-e35a-49af-b565-8d3db4bfcfed.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63629-1221-1 | 63629122101 | 2 TABLET, FILM COATED in 1 BOTTLE (63629-1221-1) | 2021-01-14 | 0000-00-00 | No | No | Current |