CHLORPHENIRAMINE MALEATE (CHLORPHENIRAMINE MALEATE) — FDA Approval ANDA080961 (AUROLIFE PHARMA LLC)
CHLORPHENIRAMINE MALEATE (CHLORPHENIRAMINE MALEATE) — FDA Approval ANDA080961 (AUROLIFE PHARMA LLC) is one of 9,000 drug approvals in the DrugApprovals dataset. Key details — Brand name: CHLORPHENIRAMINE MALEATE; Active ingredients: CHLORPHENIRAMINE MALEATE; Application number: ANDA080961.
| Brand name | CHLORPHENIRAMINE MALEATE |
|---|---|
| Active ingredients | CHLORPHENIRAMINE MALEATE |
| Application number | ANDA080961 |
| Sponsor | AUROLIFE PHARMA LLC |
| Dosage form | TABLET |
| Route | ORAL |
| Marketing status | Discontinued |
| Products in application | 1 |
| First approval date | 19721220 |
| Source | openFDA Drugs@FDA |
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