Cetirizine Hydrochloride HIVES
- Product NDC
- 57664-246
- 11-digit product format
- 576640246
- Labeler code
- 57664
- Product ID
- 57664-246_328285dd-127a-4515-8898-dfde4ac20251
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Cetirizine Hydrochloride
- Dosage form
- SOLUTION
- Route
- ORAL
- Labeler
- Caraco Pharmaceutical Laboratories, Ltd
- Application
- ANDA091327
- Marketing category
- ANDA
- Marketing start
- 2011-12-01
- Marketing end
- 0000-00-00
- Substance
- CETIRIZINE HYDROCHLORIDE
- Active strength
- 1 mg/mL
- NDC exclude flag
- E
- Listing certified through
- 2018-12-31
- Current FDA listing
- Historical FDA.report record