LORATADINE (LORATADINE) — FDA Approval ANDA211718 (HETERO LABS LTD V)
LORATADINE (LORATADINE) — FDA Approval ANDA211718 (HETERO LABS LTD V) is one of 9,000 drug approvals in the DrugApprovals dataset. Key details — Brand name: LORATADINE; Active ingredients: LORATADINE; Application number: ANDA211718.
| Brand name | LORATADINE |
|---|---|
| Active ingredients | LORATADINE |
| Application number | ANDA211718 |
| Sponsor | HETERO LABS LTD V |
| Dosage form | TABLET |
| Route | ORAL |
| Marketing status | Over-the-counter |
| Products in application | 1 |
| First approval date | 20230728 |
| Source | openFDA Drugs@FDA |
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