All Day Allergy
- Product NDC
- 62011-0408
- 11-digit product format
- 620110408
- Labeler code
- 62011
- Product ID
- 62011-0408_e99b09ef-b3d9-4fd2-9f10-40dc74a8f2b3
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Cetirizine HCL
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- McKesson (Health Mart)
- Application
- ANDA077946
- Marketing category
- ANDA
- Marketing start
- 2019-07-01
- Marketing end
- 0000-00-00
- Substance
- CETIRIZINE HYDROCHLORIDE
- Active strength
- 10 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record