All Day Allergy
- Product NDC
- 53187-220
- 11-digit product format
- 531870220
- Labeler code
- 53187
- Product ID
- 53187-220_521a2311-5b96-443e-aef1-b2f406eafb6b
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Cetirizine HCl
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- LIVE BETTER (The Great Atlantic & Pacific Tea Company)
- Application
- ANDA078427
- Marketing category
- ANDA
- Marketing start
- 2013-06-07
- 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#