Cetirizine
- Product NDC
- 11673-219
- 11-digit product format
- 116730219
- Labeler code
- 11673
- Product ID
- 11673-219_f1202eba-8b5d-c22f-e8a2-cd81a7a85755
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Cetirizine
- Dosage form
- CAPSULE, LIQUID FILLED
- Route
- ORAL
- Labeler
- TARGET CORPORATION
- Application
- ANDA207235
- Marketing category
- ANDA
- Marketing start
- 2017-12-06
- Marketing end
- 2021-11-30
- 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 | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 11673-219-02 | 11673021902 | 25 CAPSULE, LIQUID FILLED in 1 BOTTLE (11673-219-02) | 2017-12-06 | 2021-11-30 | No | No | Current |
| 11673-219-04 | 11673021904 | 40 CAPSULE, LIQUID FILLED in 1 BOTTLE (11673-219-04) | 2017-12-06 | 2021-11-30 | No | No | Current |