Claritin
- Product NDC
- 70518-2951
- 11-digit product format
- 705182951
- Labeler code
- 70518
- Product ID
- 70518-2951_d79be82a-1bed-d2b0-e053-2995a90ab00f
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Loratadine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- NDA019658
- Marketing category
- NDA
- Marketing start
- 2020-12-01
- 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
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 |
|---|
| 70518-2951-0 | 70518295100 | 1 BLISTER PACK in 1 CARTON (70518-2951-0) > 10 TABLET in 1 BLISTER PACK | 1 blister pack | 2020-12-01 | 0000-00-00 | No | No | Current |