CETIRIZINE HYDROCHLORIDE
- Product NDC
- 11822-6053
- 11-digit product format
- 118226053
- Labeler code
- 11822
- Product ID
- 11822-6053_e5d9bf97-798c-a5ea-b3a1-31da1225905c
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- CETIRIZINE HYDROCHLORIDE
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Rite Aid Corporation
- Application
- ANDA078317
- Marketing category
- ANDA
- Marketing start
- 2017-05-25
- Marketing end
- 2021-04-30
- 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 11822-6053-7 | 11822605307 | 2 BLISTER PACK in 1 CARTON (11822-6053-7) > 7 TABLET, FILM COATED in 1 BLISTER PACK | 2 blister pack | 2017-05-25 | 2021-04-30 | No | No | Current |
| 11822-6053-9 | 11822605309 | 1 BOTTLE in 1 CARTON (11822-6053-9) > 60 TABLET, FILM COATED in 1 BOTTLE | 1 bottle | 2017-05-25 | 2021-04-30 | No | No | Current |