Rite Aid
- Product NDC
- 11822-2102
- 11-digit product format
- 118222102
- Labeler code
- 11822
- Product ID
- 11822-2102_5d39f492-09a8-4d3d-a658-e34747b1188a
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Cetirizine Hydrochloride
- Dosage form
- SOLUTION
- Route
- ORAL
- Labeler
- Rite Aid Corporation
- Application
- ANDA090182
- Marketing category
- ANDA
- Marketing start
- 2011-09-08
- Marketing end
- 0000-00-00
- Substance
- CETIRIZINE HYDROCHLORIDE
- Active strength
- 5 mg/5mL
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 11822-2102 | RITE AID CHILDRENS ALLERGY RELIEF (CETIRIZINE HYDROCHLORIDE) SOLUTION [RITE AID CORPORATION] | 5 | Legacy NDC | 20210428_047a668e-bba9-4c94-91bb-140acf2bbaa0.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 11822-2102-1 | 11822210201 | 1 BOTTLE in 1 CARTON (11822-2102-1) > 240 mL in 1 BOTTLE | 1 bottle | 2012-12-12 | 0000-00-00 | No | No | Current |