Claritin-D
- Product NDC
- 70518-2761
- 11-digit product format
- 705182761
- Labeler code
- 70518
- Product ID
- 70518-2761_ec6bf1e4-6caa-5964-e053-2995a90a0aa5
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Loratadine and pseudoephedrine sulfate
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- NDA020470
- Marketing category
- NDA
- Marketing start
- 2020-05-29
- Marketing end
- 0000-00-00
- Substance
- LORATADINE; PSEUDOEPHEDRINE SULFATE
- Active strength
- 10 mg/1; mg/1
- Pharmacologic classes
- Adrenergic alpha-Agonists [MoA], alpha-Adrenergic Agonist [EPC]
- 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 |
|---|
| 70518-2761-0 | 70518276100 | 3 BLISTER PACK in 1 CARTON (70518-2761-0) > 15 TABLET, EXTENDED RELEASE in 1 BLISTER PACK | 3 blister pack | 2020-05-29 | 0000-00-00 | No | No | Current |