All Day Allergy
- Product NDC
- 62011-0205
- 11-digit product format
- 620110205
- Labeler code
- 62011
- Product ID
- 62011-0205_f0bbfbdb-dd85-4ed6-8b06-165d2b3e272b
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Cetirizine HCl
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Strategic Sourcing Services LLC
- Application
- ANDA078780
- Marketing category
- ANDA
- Marketing start
- 2012-01-01
- Marketing end
- 2020-12-30
- 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