All Day Allergy
- Product NDC
- 41520-129
- 11-digit product format
- 415200129
- Labeler code
- 41520
- Product ID
- 41520-129_935b245a-3cfc-4640-9c1a-0466971776d7
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Cetirizine HCl
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Care One (American Sales Company)
- Application
- ANDA078780
- Marketing category
- ANDA
- Marketing start
- 2010-09-07
- 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#