Loratadine
- Product NDC
- 70518-1335
- 11-digit product format
- 705181335
- Labeler code
- 70518
- Product ID
- 70518-1335_e3c7d817-8ddb-759b-e053-2995a90acadd
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Loratadine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA076301
- Marketing category
- ANDA
- Marketing start
- 2018-07-31
- Marketing end
- 0000-00-00
- Substance
- LORATADINE
- Active strength
- 10 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 70518-1335-0 | 70518133500 | 30 TABLET in 1 BOTTLE, PLASTIC (70518-1335-0) | 30 tablet | 2018-07-31 | 0000-00-00 | No | No | Current |
| 70518-1335-1 | 70518133501 | 20 TABLET in 1 BOTTLE, PLASTIC (70518-1335-1) | 20 tablet | 2018-08-08 | 0000-00-00 | No | No | Current |
| 70518-1335-3 | 70518133503 | 90 TABLET in 1 BOTTLE, PLASTIC (70518-1335-3) | 90 tablet | 2018-09-11 | 0000-00-00 | No | No | Current |