Cetirizine Hydrochloride
- Product NDC
- 68071-1988
- 11-digit product format
- 680711988
- Labeler code
- 68071
- Product ID
- 68071-1988_bc06abc5-d054-14ee-e053-2a95a90ae1c2
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Cetirizine Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals, Inc.
- 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
- 2022-12-31
- 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 |
|---|
| 68071-1988-1 | 68071198801 | 10 TABLET, FILM COATED in 1 BOTTLE (68071-1988-1) | 2017-02-21 | 0000-00-00 | No | No | Current |
| 68071-1988-3 | 68071198803 | 30 TABLET, FILM COATED in 1 BOTTLE (68071-1988-3) | 2017-02-21 | 0000-00-00 | No | No | Current |
| 68071-1988-7 | 68071198807 | 7 TABLET, FILM COATED in 1 BOTTLE (68071-1988-7) | 2017-02-21 | 0000-00-00 | No | No | Current |
| 68071-1988-9 | 68071198809 | 90 TABLET, FILM COATED in 1 BOTTLE (68071-1988-9) | 2017-02-21 | 0000-00-00 | No | No | Current |