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Drugs@FDA: FDA-Approved Drugs

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Abbreviated New Drug Application (ANDA): 200429
Company: AUROBINDO PHARMA

Products on ANDA 200429

Drug Name	Active Ingredients	Strength	Dosage Form/Route	Marketing Status	TE Code	RLD	RS
NAPROXEN	NAPROXEN	250MG	TABLET;ORAL	Prescription	AB	No	No
NAPROXEN	NAPROXEN	375MG	TABLET;ORAL	Prescription	AB	No	No
NAPROXEN	NAPROXEN	500MG	TABLET;ORAL	Prescription	AB	No	No

Approval Date(s) and History, Letters, Labels, Reviews for ANDA 200429

Original Approvals or Tentative Approvals

Action Date	Submission	Action Type	Submission Classification	Review Priority; Orphan Status	Letters, Reviews, Labels, Patient Package Insert	Notes	Url
11/08/2011	ORIG-1	Approval	Not Applicable			Label is not available on this site.

Supplements

Action Date	Submission	Supplement Categories or Approval Type	Letters, Reviews, Labels, Patient Package Insert	Note	Url
10/03/2019	SUPPL-11	Labeling-Package Insert		Label is not available on this site.
10/03/2019	SUPPL-8	Labeling-Medication Guide, Labeling-Package Insert		Label is not available on this site.
06/30/2015	SUPPL-4	Labeling-Package Insert		Label is not available on this site.

Therapeutic Equivalents for ANDA 200429

NAPROXEN

TABLET;ORAL; 250MG
TE Code = AB

Drug Name	Active Ingredients	Strength	Dosage Form/Route	Marketing Status	RLD	TE Code	Application No.	Company
NAPROXEN	NAPROXEN	250MG	TABLET;ORAL	Prescription	No	AB	075927	AMNEAL PHARMS NY
NAPROXEN	NAPROXEN	250MG	TABLET;ORAL	Prescription	No	AB	200429	AUROBINDO PHARMA
NAPROXEN	NAPROXEN	250MG	TABLET;ORAL	Prescription	No	AB	078250	GLENMARK PHARMS LTD
NAPROXEN	NAPROXEN	250MG	TABLET;ORAL	Prescription	No	AB	074140	GRANULES
NAPROXEN	NAPROXEN	250MG	TABLET;ORAL	Prescription	No	AB	091416	MARKSANS PHARMA
NAPROXEN	NAPROXEN	250MG	TABLET;ORAL	Prescription	No	AB	212517	SCIEGEN PHARMS INC
NAPROXEN	NAPROXEN	250MG	TABLET;ORAL	Prescription	No	AB	074201	TEVA
NAPROXEN	NAPROXEN	250MG	TABLET;ORAL	Prescription	No	AB	078620	ZYDUS PHARMS USA

TABLET;ORAL; 375MG
TE Code = AB

Drug Name	Active Ingredients	Strength	Dosage Form/Route	Marketing Status	RLD	TE Code	Application No.	Company
NAPROXEN	NAPROXEN	375MG	TABLET;ORAL	Prescription	No	AB	075927	AMNEAL PHARMS NY
NAPROXEN	NAPROXEN	375MG	TABLET;ORAL	Prescription	No	AB	200429	AUROBINDO PHARMA
NAPROXEN	NAPROXEN	375MG	TABLET;ORAL	Prescription	No	AB	078250	GLENMARK PHARMS LTD
NAPROXEN	NAPROXEN	375MG	TABLET;ORAL	Prescription	No	AB	074140	GRANULES
NAPROXEN	NAPROXEN	375MG	TABLET;ORAL	Prescription	No	AB	091416	MARKSANS PHARMA
NAPROXEN	NAPROXEN	375MG	TABLET;ORAL	Prescription	No	AB	212517	SCIEGEN PHARMS INC
NAPROXEN	NAPROXEN	375MG	TABLET;ORAL	Prescription	No	AB	074201	TEVA
NAPROXEN	NAPROXEN	375MG	TABLET;ORAL	Prescription	No	AB	078620	ZYDUS PHARMS USA

TABLET;ORAL; 500MG
TE Code = AB

Drug Name	Active Ingredients	Strength	Dosage Form/Route	Marketing Status	RLD	TE Code	Application No.	Company
NAPROSYN	NAPROXEN	500MG	TABLET;ORAL	Prescription	Yes	AB	017581	ATNAHS PHARMA US
NAPROXEN	NAPROXEN	500MG	TABLET;ORAL	Prescription	No	AB	075927	AMNEAL PHARMS NY
NAPROXEN	NAPROXEN	500MG	TABLET;ORAL	Prescription	No	AB	200429	AUROBINDO PHARMA
NAPROXEN	NAPROXEN	500MG	TABLET;ORAL	Prescription	No	AB	078250	GLENMARK PHARMS LTD
NAPROXEN	NAPROXEN	500MG	TABLET;ORAL	Prescription	No	AB	074140	GRANULES
NAPROXEN	NAPROXEN	500MG	TABLET;ORAL	Prescription	No	AB	091416	MARKSANS PHARMA
NAPROXEN	NAPROXEN	500MG	TABLET;ORAL	Prescription	No	AB	212517	SCIEGEN PHARMS INC
NAPROXEN	NAPROXEN	500MG	TABLET;ORAL	Prescription	No	AB	074201	TEVA
NAPROXEN	NAPROXEN	500MG	TABLET;ORAL	Prescription	No	AB	078620	ZYDUS PHARMS USA

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