Cetirizine Hydrochloride
- Product NDC
- 63629-5153
- 11-digit product format
- 636295153
- Labeler code
- 63629
- Product ID
- 63629-5153_85877234-008b-46bc-a690-8cc26e7084be
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Cetirizine Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA078317
- Marketing category
- ANDA
- Marketing start
- 2007-12-27
- Marketing end
- 0000-00-00
- Substance
- CETIRIZINE HYDROCHLORIDE
- Active strength
- 10 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63629-5153-1 | 63629515301 | 30 TABLET, FILM COATED in 1 BOTTLE (63629-5153-1) | 2008-04-03 | 0000-00-00 | No | No | Current |
| 63629-5153-2 | 63629515302 | 90 TABLET, FILM COATED in 1 BOTTLE (63629-5153-2) | 2008-04-03 | 0000-00-00 | No | No | Current |