اطلاعات داروی نمایش داده شده مستقیما از دیتابیس اطلاعات دارویی سازمان غذا و دارو آمریکا (FDA) استخراج می شود و مرتبا به روز رسانی می شود
داروی نمایش داده شده مورد تایید FDA می باشد و اطلاعات ثبت آن در زیر قابل مشاهده است
BUPRENORPHINE HYDROCHLORIDE از شرکت RUBICON
Abbreviated New Drug Application (ANDA): 090279
Company: RUBICON
| 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 |
|---|---|---|---|---|---|---|---|
| 06/10/2015 | 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 |
|---|---|---|---|---|---|
| 03/04/2021 | SUPPL-11 | Labeling-Package Insert |
Label is not available on this site. |
||
| 10/09/2019 | SUPPL-10 | 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-Package Insert |
Label is not available on this site. |
||
| 05/23/2017 | SUPPL-7 | REMS-Modified |
Label is not available on this site. |
||
| 12/16/2016 | SUPPL-6 | Labeling-Package Insert |
Label is not available on this site. |
||
| 12/16/2016 | SUPPL-5 | Labeling-Package Insert |
Label is not available on this site. |
||
| 07/07/2016 | SUPPL-4 | 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 |
حتما بخوانید : CELONTIN از شرکت PARKE DAVIS
منبع : www.accessdata.fda.gov
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