LORATADINE
- Product NDC
- 70000-0317
- 11-digit product format
- 700000317
- Labeler code
- 70000
- Product ID
- 70000-0317_5dfc16cb-6ce6-a55b-a801-d27ebb309e67
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Loratadine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Cardinal Health
- Application
- ANDA076471
- Marketing category
- ANDA
- Marketing start
- 2016-06-22
- Marketing end
- 2021-10-31
- Substance
- LORATADINE
- Active strength
- 10 mg/1
- 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70000-0317-1 | 70000031701 | 300 TABLET in 1 BOTTLE (70000-0317-1) | 300 tablet | 2016-06-23 | 2021-10-31 | No | No | Current |