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Drugs@FDA: FDA-Approved Drugs

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Abbreviated New Drug Application (ANDA): 071268
Company: CONTRACT PHARMACAL
Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status TE Code RLD RS
IBUPROFEN IBUPROFEN 600MG TABLET;ORAL Prescription AB No No
IBUPROFEN IBUPROFEN 400MG TABLET;ORAL Prescription AB No No
IBUPROFEN IBUPROFEN 800MG TABLET;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
10/15/1986 ORIG-1 Approval

Label is not available on this site.

Supplements
Action Date Submission Supplement Categories or Approval Type Letters, Reviews, Labels, Patient Package Insert Note Url
04/28/2021 SUPPL-16 Labeling-Medication Guide, Labeling-Package Insert

Label is not available on this site.

07/22/2019 SUPPL-14 Labeling-Package Insert

Label is not available on this site.

05/09/2016 SUPPL-13 Labeling-Medication Guide, Labeling-Package Insert

Label is not available on this site.

01/23/1989 SUPPL-12 Labeling

Label is not available on this site.

08/10/1988 SUPPL-11 Labeling

Label is not available on this site.

12/18/1987 SUPPL-10 Manufacturing (CMC)

Label is not available on this site.

12/18/1987 SUPPL-9 Manufacturing (CMC)

Label is not available on this site.

12/18/1987 SUPPL-8 Manufacturing (CMC)

Label is not available on this site.

07/06/1987 SUPPL-7 Manufacturing (CMC)

Label is not available on this site.

07/06/1987 SUPPL-6 Manufacturing (CMC)

Label is not available on this site.

07/06/1987 SUPPL-5 Manufacturing (CMC)

Label is not available on this site.

10/02/1987 SUPPL-4 Manufacturing (CMC)

Label is not available on this site.

01/21/1987 SUPPL-3 Manufacturing (CMC)

Label is not available on this site.

05/14/1987 SUPPL-2 Manufacturing (CMC)

Label is not available on this site.

05/14/1987 SUPPL-1 Manufacturing (CMC)

Label is not available on this site.

IBUPROFEN

TABLET;ORAL; 600MG
TE Code = AB

Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status RLD TE Code Application No. Company
IBUPROFEN IBUPROFEN 600MG TABLET;ORAL Prescription No AB 214699 ALKEM LABS LTD
IBUPROFEN IBUPROFEN 600MG TABLET;ORAL Prescription No AB 071335 AMNEAL PHARMS NY
IBUPROFEN IBUPROFEN 600MG TABLET;ORAL Prescription No AB 078558 AMNEAL PHARMS NY
IBUPROFEN IBUPROFEN 600MG TABLET;ORAL Prescription No AB 213794 AUROBINDO PHARMA LTD
IBUPROFEN IBUPROFEN 600MG TABLET;ORAL Prescription No AB 071268 CONTRACT PHARMACAL
IBUPROFEN IBUPROFEN 600MG TABLET;ORAL Prescription No AB 075682 DR REDDYS LA
IBUPROFEN IBUPROFEN 600MG TABLET;ORAL Prescription No AB 076112 DR REDDYS LABS INC
IBUPROFEN IBUPROFEN 600MG TABLET;ORAL Prescription No AB 091625 GRANULES
IBUPROFEN IBUPROFEN 600MG TABLET;ORAL Prescription No AB 090796 MARKSANS PHARMA
IBUPROFEN IBUPROFEN 600MG TABLET;ORAL Prescription No AB 202413 SHANDONG XINHUA
IBUPROFEN IBUPROFEN 600MG TABLET;ORAL Prescription No AB 078329 STRIDES PHARMA
IBUPROFEN IBUPROFEN 600MG TABLET;ORAL Prescription No AB 215318 YICHANG HUMANWELL

TABLET;ORAL; 400MG
TE Code = AB

Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status RLD TE Code Application No. Company
IBUPROFEN IBUPROFEN 400MG TABLET;ORAL Prescription No AB 214699 ALKEM LABS LTD
IBUPROFEN IBUPROFEN 400MG TABLET;ORAL Prescription No AB 071334 AMNEAL PHARMS NY
IBUPROFEN IBUPROFEN 400MG TABLET;ORAL Prescription No AB 078558 AMNEAL PHARMS NY
IBUPROFEN IBUPROFEN 400MG TABLET;ORAL Prescription No AB 213794 AUROBINDO PHARMA LTD
IBUPROFEN IBUPROFEN 400MG TABLET;ORAL Prescription No AB 071267 CONTRACT PHARMACAL
IBUPROFEN IBUPROFEN 400MG TABLET;ORAL Prescription No AB 071268 CONTRACT PHARMACAL
IBUPROFEN IBUPROFEN 400MG TABLET;ORAL Prescription No AB 075682 DR REDDYS LA
IBUPROFEN IBUPROFEN 400MG TABLET;ORAL Prescription No AB 076112 DR REDDYS LABS INC
IBUPROFEN IBUPROFEN 400MG TABLET;ORAL Prescription No AB 091625 GRANULES
IBUPROFEN IBUPROFEN 400MG TABLET;ORAL Prescription No AB 090796 MARKSANS PHARMA
IBUPROFEN IBUPROFEN 400MG TABLET;ORAL Prescription No AB 202413 SHANDONG XINHUA
IBUPROFEN IBUPROFEN 400MG TABLET;ORAL Prescription No AB 078329 STRIDES PHARMA
IBUPROFEN IBUPROFEN 400MG TABLET;ORAL Prescription No AB 215318 YICHANG HUMANWELL

TABLET;ORAL; 800MG
TE Code = AB

Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status RLD TE Code Application No. Company
IBUPROFEN IBUPROFEN 800MG TABLET;ORAL Prescription No AB 214699 ALKEM LABS LTD
IBUPROFEN IBUPROFEN 800MG TABLET;ORAL Prescription No AB 071935 AMNEAL PHARMS NY
IBUPROFEN IBUPROFEN 800MG TABLET;ORAL Prescription No AB 078558 AMNEAL PHARMS NY
IBUPROFEN IBUPROFEN 800MG TABLET;ORAL Prescription No AB 213794 AUROBINDO PHARMA LTD
IBUPROFEN IBUPROFEN 800MG TABLET;ORAL Prescription No AB 071268 CONTRACT PHARMACAL
IBUPROFEN IBUPROFEN 800MG TABLET;ORAL Prescription No AB 072300 CONTRACT PHARMACAL
IBUPROFEN IBUPROFEN 800MG TABLET;ORAL Prescription No AB 075682 DR REDDYS LA
IBUPROFEN IBUPROFEN 800MG TABLET;ORAL Prescription No AB 076112 DR REDDYS LABS INC
IBUPROFEN IBUPROFEN 800MG TABLET;ORAL Prescription No AB 091625 GRANULES
IBUPROFEN IBUPROFEN 800MG TABLET;ORAL Prescription No AB 090796 MARKSANS PHARMA
IBUPROFEN IBUPROFEN 800MG TABLET;ORAL Prescription No AB 202413 SHANDONG XINHUA
IBUPROFEN IBUPROFEN 800MG TABLET;ORAL Prescription No AB 078329 STRIDES PHARMA
IBUPROFEN IBUPROFEN 800MG TABLET;ORAL Prescription No AB 215318 YICHANG HUMANWELL
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