Loratadine
- Product NDC
- 61715-017
- 11-digit product format
- 617150017
- Labeler code
- 61715
- Product ID
- 61715-017_de98b206-8dbe-42f1-82ac-8c1f92a9e1af
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Loratadine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Kinray
- Application
- ANDA076134
- Marketing category
- ANDA
- Marketing start
- 2003-08-19
- Marketing end
- 0000-00-00
- Substance
- LORATADINE
- Active strength
- 10 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 61715-017-30 | 2025-05-27 | C162847 | 48780-1 | 9d75b9d0-b4a0-f424-e053-dadaa90a57ce | e00398de-e20b-481b-922b-36b37020b827 |
| 61715-017-51 | 2025-05-27 | C162847 | 48780-1 | 9d75b9d0-b4a0-f424-e053-dadaa90a57ce | e00398de-e20b-481b-922b-36b37020b827 |
| 61715-017-30 | 2020-01-31 | C162847 | 48780-1 | 9d75b9d0-b4a0-f424-e053-dadaa90a57ce | e00398de-e20b-481b-922b-36b37020b827 |
| 61715-017-51 | 2020-01-31 | C162847 | 48780-1 | 9d75b9d0-b4a0-f424-e053-dadaa90a57ce | e00398de-e20b-481b-922b-36b37020b827 |