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Drugs@FDA: FDA-Approved Drugs

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Abbreviated New Drug Application (ANDA): 215311
Company: STRIDES PHARMA
Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status TE Code RLD RS
IBUPROFEN IBUPROFEN 100MG/5ML SUSPENSION;ORAL Prescription AB No No
Original Approvals or Tentative Approvals
Action Date Submission Action Type Submission Classification Review Priority; Orphan Status Letters, Reviews, Labels, Patient Package Insert Notes Url
05/27/2022 ORIG-1 Approval STANDARD

Label is not available on this site.

IBUPROFEN

SUSPENSION;ORAL; 100MG/5ML
TE Code = AB

Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status RLD TE Code Application No. Company
IBUPROFEN IBUPROFEN 100MG/5ML SUSPENSION;ORAL Prescription No AB 074978 ACTAVIS MID ATLANTIC
IBUPROFEN IBUPROFEN 100MG/5ML SUSPENSION;ORAL Prescription No AB 209178 AUROBINDO PHARMA LTD
IBUPROFEN IBUPROFEN 100MG/5ML SUSPENSION;ORAL Prescription No AB 076925 PADAGIS US
IBUPROFEN IBUPROFEN 100MG/5ML SUSPENSION;ORAL Prescription No AB 215311 STRIDES PHARMA
IBUPROFEN IBUPROFEN 100MG/5ML SUSPENSION;ORAL Prescription No AB 209204 TARO
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