Cetirizine
- Product NDC
- 60505-4668
- 11-digit product format
- 605054668
- Labeler code
- 60505
- Product ID
- 60505-4668_c7ca2e17-5968-18b0-8d37-8bf875adc114
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Cetirizine
- Dosage form
- CAPSULE, LIQUID FILLED
- Route
- ORAL
- Labeler
- Apotex Corp.
- Application
- ANDA207235
- Marketing category
- ANDA
- Marketing start
- 2018-04-18
- Marketing end
- 2022-05-31
- 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 60505-4668-6 | 60505466806 | 1 BOTTLE in 1 CARTON (60505-4668-6) > 65 CAPSULE, LIQUID FILLED in 1 BOTTLE | 1 bottle | 2018-04-18 | 2022-05-31 | No | No | Current |