Cetirizine Hydrochloride
- Product NDC
- 60505-2632
- 11-digit product format
- 605052632
- Labeler code
- 60505
- Product ID
- 60505-2632_17fe6683-fe11-595a-7f5b-08127105a627
- 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
- 2007-12-27
- Marketing end
- 2021-04-30
- Substance
- CETIRIZINE HYDROCHLORIDE
- Active strength
- 5 mg/1
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 60505-2632-1 | 60505263201 | 100 TABLET, FILM COATED in 1 BOTTLE (60505-2632-1) | 2007-12-27 | 2021-04-30 | No | No | Current |
| 60505-2632-3 | 60505263203 | 30 TABLET, FILM COATED in 1 BOTTLE (60505-2632-3) | 2007-12-27 | 2021-04-30 | No | No | Current |
| 60505-2632-8 | 60505263208 | 1000 TABLET, FILM COATED in 1 BOTTLE (60505-2632-8) | 2007-12-27 | 2021-04-30 | No | No | Current |