CETIRIZINE HYDROCHLORIDE
- Product NDC
- 60505-4650
- 11-digit product format
- 605054650
- Labeler code
- 60505
- Product ID
- 60505-4650_cbad0bf7-8a32-c14d-6304-7ed3b0c95bdb
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- CETIRIZINE HYDROCHLORIDE
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Apotex Corp.
- Application
- ANDA078317
- Marketing category
- ANDA
- Marketing start
- 2018-02-06
- Marketing end
- 2020-12-31
- Substance
- CETIRIZINE HYDROCHLORIDE
- Active strength
- 10 mg/1
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record