Albendazole
- Product NDC
- 62980-513
- 11-digit product format
- 629800513
- Labeler code
- 62980
- Product ID
- 62980-513_b8b8fc38-4662-467c-8a2e-ba76117c009b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Albendazole
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Vivimed Labs USA
- 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
- 2020-12-31
- Current FDA listing
- Historical FDA.report record