all day allergy
- Product NDC
- 62011-0313
- 11-digit product format
- 620110313
- Labeler code
- 62011
- Product ID
- 62011-0313_16152ff4-adac-4f2e-aae4-8b6b039cd3ab
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Cetirizine HCl
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Strategic Sourcing Services LLC
- Application
- ANDA090760
- Marketing category
- ANDA
- Marketing start
- 2015-08-05
- Marketing end
- 2020-11-30
- 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