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
ALENDRONATE SODIUM از شرکت SUN PHARM
Abbreviated New Drug Application (ANDA): 090022
Company: SUN PHARM
Drug Name | Active Ingredients | Strength | Dosage Form/Route | Marketing Status | TE Code | RLD | RS |
---|---|---|---|---|---|---|---|
ALENDRONATE SODIUM | ALENDRONATE SODIUM | EQ 5MG BASE | TABLET;ORAL | Prescription |
AB |
No | No |
ALENDRONATE SODIUM | ALENDRONATE SODIUM | EQ 10MG BASE | TABLET;ORAL | Prescription |
AB |
No | No |
ALENDRONATE SODIUM | ALENDRONATE SODIUM | EQ 35MG BASE | TABLET;ORAL | Prescription |
AB |
No | No |
ALENDRONATE SODIUM | ALENDRONATE SODIUM | EQ 70MG BASE | 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 |
---|---|---|---|---|---|---|---|
09/10/2008 | 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 |
---|---|---|---|---|---|
04/08/2016 | SUPPL-12 | Labeling-Package Insert |
Label is not available on this site. |
||
09/29/2015 | SUPPL-11 | Labeling-Package Insert |
Label is not available on this site. |
||
09/29/2015 | SUPPL-9 | Labeling-Package Insert |
Label is not available on this site. |
||
05/07/2013 | SUPPL-8 | Labeling-Package Insert |
Label is not available on this site. |
||
11/28/2012 | SUPPL-7 | Labeling-Package Insert |
Label is not available on this site. |
||
12/01/2011 | SUPPL-6 | REMS-Proposal |
Label is not available on this site. |
||
04/05/2011 | SUPPL-5 | Labeling-Package Insert, REMS-Proposal |
Label is not available on this site. |
||
11/29/2010 | SUPPL-4 | Labeling-Patient Package Insert, Labeling-Package Insert |
Label is not available on this site. |
||
11/17/2009 | SUPPL-2 | Labeling-Container/Carton Labels |
Label is not available on this site. |
ALENDRONATE SODIUM
TABLET;ORAL; EQ 5MG BASE
TE Code = AB
Drug Name | Active Ingredients | Strength | Dosage Form/Route | Marketing Status | RLD | TE Code | Application No. | Company |
---|---|---|---|---|---|---|---|---|
ALENDRONATE SODIUM | ALENDRONATE SODIUM | EQ 5MG BASE | TABLET;ORAL | Prescription | No | AB | 077982 | APOTEX |
ALENDRONATE SODIUM | ALENDRONATE SODIUM | EQ 5MG BASE | TABLET;ORAL | Prescription | No | AB | 076768 | CIPLA |
ALENDRONATE SODIUM | ALENDRONATE SODIUM | EQ 5MG BASE | TABLET;ORAL | Prescription | No | AB | 090258 | HANGZHOU BINJIANG |
ALENDRONATE SODIUM | ALENDRONATE SODIUM | EQ 5MG BASE | TABLET;ORAL | Prescription | No | AB | 075710 | IMPAX LABS INC |
ALENDRONATE SODIUM | ALENDRONATE SODIUM | EQ 5MG BASE | TABLET;ORAL | Prescription | No | AB | 090022 | SUN PHARM |
TABLET;ORAL; EQ 10MG BASE
TE Code = AB
Drug Name | Active Ingredients | Strength | Dosage Form/Route | Marketing Status | RLD | TE Code | Application No. | Company |
---|---|---|---|---|---|---|---|---|
ALENDRONATE SODIUM | ALENDRONATE SODIUM | EQ 10MG BASE | TABLET;ORAL | Prescription | No | AB | 077982 | APOTEX |
ALENDRONATE SODIUM | ALENDRONATE SODIUM | EQ 10MG BASE | TABLET;ORAL | Prescription | No | AB | 090124 | AUROBINDO PHARMA |
ALENDRONATE SODIUM | ALENDRONATE SODIUM | EQ 10MG BASE | TABLET;ORAL | Prescription | No | AB | 076768 | CIPLA |
ALENDRONATE SODIUM | ALENDRONATE SODIUM | EQ 10MG BASE | TABLET;ORAL | Prescription | No | AB | 090258 | HANGZHOU BINJIANG |
ALENDRONATE SODIUM | ALENDRONATE SODIUM | EQ 10MG BASE | TABLET;ORAL | Prescription | No | AB | 075710 | IMPAX LABS INC |
ALENDRONATE SODIUM | ALENDRONATE SODIUM | EQ 10MG BASE | TABLET;ORAL | Prescription | No | AB | 090022 | SUN PHARM |
TABLET;ORAL; EQ 35MG BASE
TE Code = AB
Drug Name | Active Ingredients | Strength | Dosage Form/Route | Marketing Status | RLD | TE Code | Application No. | Company |
---|---|---|---|---|---|---|---|---|
ALENDRONATE SODIUM | ALENDRONATE SODIUM | EQ 35MG BASE | TABLET;ORAL | Prescription | No | AB | 077982 | APOTEX |
ALENDRONATE SODIUM | ALENDRONATE SODIUM | EQ 35MG BASE | TABLET;ORAL | Prescription | No | AB | 090124 | AUROBINDO PHARMA |
ALENDRONATE SODIUM | ALENDRONATE SODIUM | EQ 35MG BASE | TABLET;ORAL | Prescription | No | AB | 076768 | CIPLA |
ALENDRONATE SODIUM | ALENDRONATE SODIUM | EQ 35MG BASE | TABLET;ORAL | Prescription | No | AB | 090258 | HANGZHOU BINJIANG |
ALENDRONATE SODIUM | ALENDRONATE SODIUM | EQ 35MG BASE | TABLET;ORAL | Prescription | No | AB | 075710 | IMPAX LABS INC |
ALENDRONATE SODIUM | ALENDRONATE SODIUM | EQ 35MG BASE | TABLET;ORAL | Prescription | No | AB | 090022 | SUN PHARM |
ALENDRONATE SODIUM | ALENDRONATE SODIUM | EQ 35MG BASE | TABLET;ORAL | Prescription | No | AB | 076984 | WATSON LABS |
TABLET;ORAL; EQ 70MG BASE
TE Code = AB
Drug Name | Active Ingredients | Strength | Dosage Form/Route | Marketing Status | RLD | TE Code | Application No. | Company |
---|---|---|---|---|---|---|---|---|
ALENDRONATE SODIUM | ALENDRONATE SODIUM | EQ 70MG BASE | TABLET;ORAL | Prescription | No | AB | 077982 | APOTEX |
ALENDRONATE SODIUM | ALENDRONATE SODIUM | EQ 70MG BASE | TABLET;ORAL | Prescription | No | AB | 090124 | AUROBINDO PHARMA |
ALENDRONATE SODIUM | ALENDRONATE SODIUM | EQ 70MG BASE | TABLET;ORAL | Prescription | No | AB | 076768 | CIPLA |
ALENDRONATE SODIUM | ALENDRONATE SODIUM | EQ 70MG BASE | TABLET;ORAL | Prescription | No | AB | 090258 | HANGZHOU BINJIANG |
ALENDRONATE SODIUM | ALENDRONATE SODIUM | EQ 70MG BASE | TABLET;ORAL | Prescription | No | AB | 075710 | IMPAX LABS INC |
ALENDRONATE SODIUM | ALENDRONATE SODIUM | EQ 70MG BASE | TABLET;ORAL | Prescription | No | AB | 090022 | SUN PHARM |
ALENDRONATE SODIUM | ALENDRONATE SODIUM | EQ 70MG BASE | TABLET;ORAL | Prescription | No | AB | 076984 | WATSON LABS |
FOSAMAX | ALENDRONATE SODIUM | EQ 70MG BASE | TABLET;ORAL | Prescription | Yes | AB | 020560 | MERCK AND CO INC |
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