up and up childrens allergy
- Product NDC
- 82442-617
- 11-digit product format
- 824420617
- Labeler code
- 82442
- Product ID
- 82442-617_b0ae7da4-e25b-4ff3-995a-ce3add69c6c2
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Cetirizine Hydrochloride
- Dosage form
- SOLUTION
- Route
- ORAL
- Labeler
- Target Corporation
- Application
- ANDA204226
- Marketing category
- ANDA
- Marketing start
- 2024-06-04
- Substance
- CETIRIZINE HYDROCHLORIDE
- Active strength
- 5 mg/5mL
- Pharmacologic classes
- Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 64O047KTOA | CETIRIZINE HYDROCHLORIDE | 83881-52-1 | CETIRIZINE HYDROCHLORIDE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 82442-617-26 | 82442061726 | 1 BOTTLE in 1 CARTON (82442-617-26) / 118 mL in 1 BOTTLE | 1 bottle | 2024-06-04 | No | No | Historical |