Loratadine
- Product NDC
- 68788-8659
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Loratadine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA210722
- Marketing category
- ANDA
- Substance
- LORATADINE
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 68788-8659-0 | 10 TABLET in 1 BOTTLE (68788-8659-0) | 20240513 | | No | Historical |
| 68788-8659-1 | 14 TABLET in 1 BOTTLE (68788-8659-1) | 20240513 | | No | Historical |
| 68788-8659-3 | 30 TABLET in 1 BOTTLE (68788-8659-3) | 20240513 | | No | Historical |
| 68788-8659-5 | 15 TABLET in 1 BOTTLE (68788-8659-5) | 20240513 | | No | Historical |
| 68788-8659-9 | 90 TABLET in 1 BOTTLE (68788-8659-9) | 20240513 | | No | Historical |