All Day Allergy Relief
- Product NDC
- 59726-024
- 11-digit product format
- 597260024
- Labeler code
- 59726
- Product ID
- 59726-024_9092ec06-416f-49cc-a499-21743af62c22
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Cetirizine HCl
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- P & L Development, LLC
- Application
- ANDA078780
- Marketing category
- ANDA
- Marketing start
- 2014-07-31
- Marketing end
- 2020-12-31
- Substance
- CETIRIZINE HYDROCHLORIDE
- Active strength
- 10 mg/1
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record