Loratadine
- Product NDC
- 68071-4121
- 11-digit product format
- 680714121
- Labeler code
- 68071
- Product ID
- 68071-4121_bc06724b-64fe-b87c-e053-2a95a90a81e0
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Loratadine
- Dosage form
- SOLUTION
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA077421
- Marketing category
- ANDA
- Marketing start
- 2011-02-17
- Marketing end
- 0000-00-00
- Substance
- LORATADINE
- 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#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68071-4121-1 | 68071412101 | 120 mL in 1 BOX (68071-4121-1) | 120 ml | 2017-10-16 | 0000-00-00 | No | No | Current |
| 68071-4121-4 | 68071412104 | 118 mL in 1 BOX (68071-4121-4) | 118 ml | 2017-10-16 | 0000-00-00 | No | No | Current |