LEADER ALL DAY ALLERGY
- Product NDC
- 37205-820
- 11-digit product format
- 372050820
- Labeler code
- 37205
- Product ID
- 37205-820_c69e021b-e6d3-4e71-9208-0d981b58e724
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- cetirizine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Cardinal Health
- Application
- ANDA077498
- Marketing category
- ANDA
- Marketing start
- 2007-12-27
- Marketing end
- 0000-00-00
- Substance
- CETIRIZINE HYDROCHLORIDE
- Active strength
- 10 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#