LORATADINE
- Product NDC
- 68788-7085
- 11-digit product format
- 687887085
- Labeler code
- 68788
- Product ID
- 68788-7085_66ec5806-0fa8-4b64-b387-e56964444269
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Loratadine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA076471
- Marketing category
- ANDA
- Marketing start
- 2018-01-25
- Marketing end
- 0000-00-00
- Substance
- LORATADINE
- Active strength
- 10 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68788-7085-0 | 68788708500 | 10 TABLET in 1 BOTTLE (68788-7085-0) | 10 tablet | 2018-01-25 | 0000-00-00 | No | No | Current |
| 68788-7085-1 | 68788708501 | 14 TABLET in 1 BOTTLE (68788-7085-1) | 14 tablet | 2018-01-25 | 0000-00-00 | No | No | Current |
| 68788-7085-3 | 68788708503 | 30 TABLET in 1 BOTTLE (68788-7085-3) | 30 tablet | 2018-01-25 | 0000-00-00 | No | No | Current |
| 68788-7085-5 | 68788708505 | 15 TABLET in 1 BOTTLE (68788-7085-5) | 15 tablet | 2018-01-25 | 0000-00-00 | No | No | Current |
| 68788-7085-9 | 68788708509 | 90 TABLET in 1 BOTTLE (68788-7085-9) | 90 tablet | 2018-01-25 | 0000-00-00 | No | No | Current |