IBUPROFEN AND PHENYLEPHRINE HYDROCHLORIDE (IBUPROFEN; PHENYLEPHRINE HYDROCHLORIDE) — FDA Approval ANDA203200 (PERRIGO R AND D)
IBUPROFEN AND PHENYLEPHRINE HYDROCHLORIDE (IBUPROFEN; PHENYLEPHRINE HYDROCHLORIDE) — FDA Approval ANDA203200 (PERRIGO R AND D) is one of 9,000 drug approvals in the DrugApprovals dataset. Key details — Brand name: IBUPROFEN AND PHENYLEPHRINE HYDROCHLORIDE; Active ingredients: IBUPROFEN; PHENYLEPHRINE HYDROCHLORIDE; App
| Brand name | IBUPROFEN AND PHENYLEPHRINE HYDROCHLORIDE |
|---|---|
| Active ingredients | IBUPROFEN; PHENYLEPHRINE HYDROCHLORIDE |
| Application number | ANDA203200 |
| Sponsor | PERRIGO R AND D |
| Dosage form | TABLET |
| Route | ORAL |
| Marketing status | Over-the-counter |
| Products in application | 1 |
| First approval date | 20140703 |
| Source | openFDA Drugs@FDA |
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