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Drugs@FDA: FDA-Approved Drugs

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Abbreviated New Drug Application (ANDA): 208834
Company: AMNEAL PHARMS CO
Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status TE Code RLD RS
ETODOLAC ETODOLAC 400MG TABLET;ORAL Prescription AB No No
ETODOLAC ETODOLAC 500MG 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
06/07/2018 ORIG-1 Approval STANDARD

Label is not available on this site.

Supplements
Action Date Submission Supplement Categories or Approval Type Letters, Reviews, Labels, Patient Package Insert Note Url
03/15/2024 SUPPL-7 Labeling-Container/Carton Labels, Labeling-Medication Guide, Labeling-Package Insert

Label is not available on this site.

04/28/2021 SUPPL-5 Labeling-Medication Guide, Labeling-Package Insert

Label is not available on this site.

ETODOLAC

TABLET;ORAL; 400MG
TE Code = AB

Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status RLD TE Code Application No. Company
ETODOLAC ETODOLAC 400MG TABLET;ORAL Prescription No AB 208834 AMNEAL PHARMS CO
ETODOLAC ETODOLAC 400MG TABLET;ORAL Prescription No AB 076004 APOTEX INC
ETODOLAC ETODOLAC 400MG TABLET;ORAL Prescription No AB 210704 BAYSHORE PHARMS LLC
ETODOLAC ETODOLAC 400MG TABLET;ORAL Prescription No AB 074903 SANDOZ
ETODOLAC ETODOLAC 400MG TABLET;ORAL Prescription No AB 075074 TARO PHARM INDS

TABLET;ORAL; 500MG
TE Code = AB

Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status RLD TE Code Application No. Company
ETODOLAC ETODOLAC 500MG TABLET;ORAL Prescription No AB 208834 AMNEAL PHARMS CO
ETODOLAC ETODOLAC 500MG TABLET;ORAL Prescription No AB 076004 APOTEX INC
ETODOLAC ETODOLAC 500MG TABLET;ORAL Prescription No AB 210704 BAYSHORE PHARMS LLC
ETODOLAC ETODOLAC 500MG TABLET;ORAL Prescription No AB 074903 SANDOZ
ETODOLAC ETODOLAC 500MG TABLET;ORAL Prescription No AB 075074 TARO PHARM INDS
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