ALBENZA
- Product NDC
- 55695-021
- 11-digit product format
- 556950021
- Labeler code
- 55695
- Product ID
- 55695-021_6179baa4-9516-4e21-e053-2991aa0ae033
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- albendazole
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Department of State Health Services, Pharmacy Branch
- Application
- NDA020666
- Marketing category
- NDA
- Marketing start
- 1996-06-11
- Marketing end
- 2019-09-30
- Substance
- ALBENDAZOLE
- Active strength
- 200 mg/1
- Pharmacologic classes
- Anthelmintic [EPC],Cytochrome P450 1A Inducers [MoA]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record