Allergy
- Product NDC
- 41250-539
- 11-digit product format
- 412500539
- Labeler code
- 41250
- Product ID
- 41250-539_40ac8d6b-776d-4c02-a735-a81bfd0bc174
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Loratadine
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- MEIJER, INC.
- Application
- ANDA077421
- Marketing category
- ANDA
- Marketing start
- 2018-02-28
- Marketing end
- 2025-02-28
- 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 |
|---|
| 41250-539-04 | 41250053904 | 1 BOTTLE, PLASTIC in 1 BOX (41250-539-04) > 120 mL in 1 BOTTLE, PLASTIC | 2018-02-28 | 2025-02-28 | No | No | Current |