Childrens Allergy
- Product NDC
- 55910-539
- 11-digit product format
- 559100539
- Labeler code
- 55910
- Product ID
- 55910-539_de9cab09-a73a-4a1c-a87e-49d4a396e7d7
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Loratadine
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Dolgencorp, Inc. (DOLLAR GENERAL & REXALL)
- Application
- ANDA077421
- Marketing category
- ANDA
- Marketing start
- 2016-02-29
- Marketing end
- 2024-01-12
- Substance
- LORATADINE
- Active strength
- 5 mg/5mL
- 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 |
|---|
| 55910-539-04 | 55910053904 | 1 BOTTLE, PLASTIC in 1 BOX (55910-539-04) > 120 mL in 1 BOTTLE, PLASTIC | 2016-02-29 | 0000-00-00 | No | No | Current |