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BUPRENORPHINE HYDROCHLORIDE از شرکت SUN PHARM

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داروی نمایش داده شده مورد تایید FDA می باشد و اطلاعات ثبت آن در زیر قابل مشاهده است

BUPRENORPHINE HYDROCHLORIDE از شرکت SUN PHARM

Abbreviated New Drug Application (ANDA): 201760

Company: SUN PHARM

Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status TE Code RLD RS
BUPRENORPHINE HYDROCHLORIDE BUPRENORPHINE HYDROCHLORIDE EQ 2MG BASE TABLET;SUBLINGUAL Prescription

AB

No No
BUPRENORPHINE HYDROCHLORIDE BUPRENORPHINE HYDROCHLORIDE EQ 8MG BASE TABLET;SUBLINGUAL 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
01/29/2016 ORIG-1 Approval

Not Applicable

Letter (PDF)

Label is not available on this site.

https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2016/201760Orig1s000ltr.pdf

Supplements
Action Date Submission Supplement Categories or Approval Type Letters, Reviews, Labels, Patient Package Insert Note Url
03/04/2021 SUPPL-18 Labeling-Package Insert, Labeling-Medication Guide

Label is not available on this site.

02/16/2021 SUPPL-15 Labeling-Package Insert, Labeling-Medication Guide

Label is not available on this site.

10/09/2019 SUPPL-12 Labeling-Package Insert

Label is not available on this site.

10/31/2018 SUPPL-9 REMS – MODIFIED – D-N-A

Label is not available on this site.

02/01/2018 SUPPL-8 Labeling-Medication Guide, Labeling-Package Insert

Label is not available on this site.

01/31/2018 SUPPL-7 Labeling-Package Insert

Label is not available on this site.

05/23/2017 SUPPL-6 REMS-Modified

Label is not available on this site.

03/24/2017 SUPPL-5 Labeling-Package Insert

Label is not available on this site.

07/07/2016 SUPPL-1 REMS-Modified

Label is not available on this site.

BUPRENORPHINE HYDROCHLORIDE

TABLET;SUBLINGUAL; EQ 2MG BASE

TE Code = AB

Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status RLD TE Code Application No. Company
BUPRENORPHINE HYDROCHLORIDE BUPRENORPHINE HYDROCHLORIDE EQ 2MG BASE TABLET;SUBLINGUAL Prescription No AB 090819 ACTAVIS ELIZABETH
BUPRENORPHINE HYDROCHLORIDE BUPRENORPHINE HYDROCHLORIDE EQ 2MG BASE TABLET;SUBLINGUAL Prescription No AB 090622 ETHYPHARM
BUPRENORPHINE HYDROCHLORIDE BUPRENORPHINE HYDROCHLORIDE EQ 2MG BASE TABLET;SUBLINGUAL Prescription No AB 078633 HIKMA
BUPRENORPHINE HYDROCHLORIDE BUPRENORPHINE HYDROCHLORIDE EQ 2MG BASE TABLET;SUBLINGUAL Prescription No AB 207276 RHODES PHARMS
BUPRENORPHINE HYDROCHLORIDE BUPRENORPHINE HYDROCHLORIDE EQ 2MG BASE TABLET;SUBLINGUAL Prescription No AB 090279 RUBICON
BUPRENORPHINE HYDROCHLORIDE BUPRENORPHINE HYDROCHLORIDE EQ 2MG BASE TABLET;SUBLINGUAL Prescription No AB 201760 SUN PHARM

TABLET;SUBLINGUAL; EQ 8MG BASE

TE Code = AB

Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status RLD TE Code Application No. Company
BUPRENORPHINE HYDROCHLORIDE BUPRENORPHINE HYDROCHLORIDE EQ 8MG BASE TABLET;SUBLINGUAL Prescription No AB 090819 ACTAVIS ELIZABETH
BUPRENORPHINE HYDROCHLORIDE BUPRENORPHINE HYDROCHLORIDE EQ 8MG BASE TABLET;SUBLINGUAL Prescription No AB 090622 ETHYPHARM
BUPRENORPHINE HYDROCHLORIDE BUPRENORPHINE HYDROCHLORIDE EQ 8MG BASE TABLET;SUBLINGUAL Prescription No AB 078633 HIKMA
BUPRENORPHINE HYDROCHLORIDE BUPRENORPHINE HYDROCHLORIDE EQ 8MG BASE TABLET;SUBLINGUAL Prescription No AB 207276 RHODES PHARMS
BUPRENORPHINE HYDROCHLORIDE BUPRENORPHINE HYDROCHLORIDE EQ 8MG BASE TABLET;SUBLINGUAL Prescription No AB 090279 RUBICON
BUPRENORPHINE HYDROCHLORIDE BUPRENORPHINE HYDROCHLORIDE EQ 8MG BASE TABLET;SUBLINGUAL Prescription No AB 201760 SUN PHARM
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