all day allergy relief
- Product NDC
- 37808-550
- 11-digit product format
- 378080550
- Labeler code
- 37808
- Product ID
- 37808-550_c6efdde5-76c9-447d-bf6e-6fba9ea34721
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Cetirizine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- H E B
- Application
- ANDA078336
- Marketing category
- ANDA
- Marketing start
- 2014-02-08
- 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