UP AND UP CHILDRENS ALLERGY
- Product NDC
- 82442-207
- 11-digit product format
- 824420207
- Labeler code
- 82442
- Product ID
- 82442-207_36a8b979-6403-4545-82e0-d3bccdd2654e
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Loratadine
- Dosage form
- SOLUTION
- Route
- ORAL
- Labeler
- Target Corporation
- Application
- ANDA075728
- Marketing category
- ANDA
- Marketing start
- 2024-07-31
- Substance
- LORATADINE
- Active strength
- 5 mg/5mL
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 7AJO3BO7QN | LORATADINE | 79794-75-5 | LORATADINE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 82442-207-26 | 82442020726 | 1 BOTTLE in 1 CARTON (82442-207-26) / 120 mL in 1 BOTTLE | 1 bottle | 2024-07-31 | No | No | Historical |