Albendazole
- Product NDC
- 31722-935
- 11-digit product format
- 317220935
- Labeler code
- 31722
- Product ID
- 31722-935_e8325090-6671-4058-8b1a-39c16ea4dc47
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Albendazole
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Camber Pharmaceuticals
- 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 Product Concepts#
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 |
|---|
| 31722-935-02 | 31722093502 | 2 TABLET, FILM COATED in 1 BOTTLE (31722-935-02) | 2018-12-15 | 0000-00-00 | No | No | Current |
| 31722-935-28 | 31722093528 | 28 TABLET, FILM COATED in 1 BOTTLE (31722-935-28) | 2018-12-15 | 0000-00-00 | No | No | Current |