Cetirizine Hydrochloride
- Product NDC
- 57451-5067
- 11-digit product format
- 574515067
- Labeler code
- 57451
- Product ID
- 57451-5067_6f2ce1a0-e50d-4feb-9b52-e70fca156c7e
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Cetirizine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Ipca Laboratories Limited
- Application
- ANDA077498
- Marketing category
- ANDA
- Marketing start
- 2007-12-27
- Marketing end
- 0000-00-00
- Substance
- CETIRIZINE HYDROCHLORIDE
- Active strength
- 10 mg/1
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#