Drugs@FDA: FDA-Approved Drugs
New Drug Application (NDA): 021908
Company: SUCAMPO PHARMA LLC
Company: SUCAMPO PHARMA LLC
Drug Name | Active Ingredients | Strength | Dosage Form/Route | Marketing Status | TE Code | RLD | RS |
---|---|---|---|---|---|---|---|
AMITIZA | LUBIPROSTONE | 24MCG | CAPSULE;ORAL | Prescription | AB | Yes | Yes |
AMITIZA | LUBIPROSTONE | 8MCG | CAPSULE;ORAL | Prescription | AB | Yes | 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 |
---|---|---|---|---|---|---|---|
01/31/2006 | ORIG-1 | Approval | Type 1 - New Molecular Entity | STANDARD |
Label (PDF)
Letter (PDF) Review |
https://www.accessdata.fda.gov/drugsatfda_docs/label/2006/021908s000lbl.pdf https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2006/021908s000ltr.pdf https://www.accessdata.fda.gov/drugsatfda_docs/nda/2006/021908s000_AmitizaTOC.cfm |
Supplements
Action Date | Submission | Supplement Categories or Approval Type | Letters, Reviews, Labels, Patient Package Insert | Note | Url |
---|---|---|---|---|---|
11/30/2020 | SUPPL-18 | Labeling-Package Insert |
Label (PDF)
Letter (PDF) |
https://www.accessdata.fda.gov/drugsatfda_docs/label/2020/021908s018lbl.pdf https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2020/021908Orig1s018ltr.pdf | |
04/26/2018 | SUPPL-16 | Efficacy-New Indication |
Label (PDF)
Letter (PDF) |
https://www.accessdata.fda.gov/drugsatfda_docs/label/2018/021908s016lbl.pdf https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2018/021908Orig1s016Ltr.pdf | |
08/01/2017 | SUPPL-15 | Labeling-Package Insert |
Label (PDF)
Letter (PDF) |
https://www.accessdata.fda.gov/drugsatfda_docs/label/2017/021908s015lbl.pdf https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2017/021908Orig1s015ltr.pdf | |
10/11/2016 | SUPPL-13 | Labeling-Package Insert |
Label (PDF)
Letter (PDF) |
https://www.accessdata.fda.gov/drugsatfda_docs/label/2016/021908s013lbl.pdf https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2016/021908Orig1s013ltr.pdf | |
08/19/2013 | SUPPL-12 | Manufacturing (CMC) |
Label is not available on this site. |
||
04/19/2013 | SUPPL-11 | Efficacy-New Indication |
Label (PDF)
Letter (PDF) Review (PDF) |
https://www.accessdata.fda.gov/drugsatfda_docs/label/2013/021908s011lbl.pdf https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2013/021908Orig1s011ltr.pdf https://www.accessdata.fda.gov/drugsatfda_docs/nda/2013/021908Orig1s011.pdf | |
11/26/2012 | SUPPL-10 | Labeling-Package Insert |
Label (PDF)
Letter (PDF) Review (PDF) |
https://www.accessdata.fda.gov/drugsatfda_docs/label/2012/021908s010lbl.pdf https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2012/021908Orig1s010ltr.pdf https://www.accessdata.fda.gov/drugsatfda_docs/nda/2012/021908Orig1s010.pdf | |
02/24/2011 | SUPPL-8 | Labeling |
Label (PDF)
Letter (PDF) Review (PDF) |
https://www.accessdata.fda.gov/drugsatfda_docs/label/2011/021908s008lbl.pdf https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2011/021908s008ltr.pdf https://www.accessdata.fda.gov/drugsatfda_docs/nda/2011/021908Orig1s008.pdf | |
04/29/2008 | SUPPL-5 | Efficacy-New Indication |
Label (PDF)
Letter (PDF) Review Summary Review (PDF) |
https://www.accessdata.fda.gov/drugsatfda_docs/label/2008/021908s005lbl.pdf https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2008/021908se1-005ltr.pdf https://www.accessdata.fda.gov/drugsatfda_docs/nda/2008/021908s005TOC.cfm https://www.accessdata.fda.gov/drugsatfda_docs/summary_review/2008/021908se1-005_SUMR.pdf | |
05/16/2007 | SUPPL-4 | Labeling |
Label (PDF)
Letter (PDF) |
https://www.accessdata.fda.gov/drugsatfda_docs/label/2007/021908s004lbl.pdf https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2007/021908s004ltr.pdf |
Action Date | Submission | Supplement Categories or Approval Type | Letters, Reviews, Labels, Patient Package Insert |
Note | Url |
---|---|---|---|---|---|
11/30/2020 | SUPPL-18 | Labeling-Package Insert | Label (PDF) | https://www.accessdata.fda.gov/drugsatfda_docs/label/2020/021908s018lbl.pdf | |
04/26/2018 | SUPPL-16 | Efficacy-New Indication | Label (PDF) | https://www.accessdata.fda.gov/drugsatfda_docs/label/2018/021908s016lbl.pdf | |
08/01/2017 | SUPPL-15 | Labeling-Package Insert | Label (PDF) | https://www.accessdata.fda.gov/drugsatfda_docs/label/2017/021908s015lbl.pdf | |
10/11/2016 | SUPPL-13 | Labeling-Package Insert | Label (PDF) | https://www.accessdata.fda.gov/drugsatfda_docs/label/2016/021908s013lbl.pdf | |
04/19/2013 | SUPPL-11 | Efficacy-New Indication | Label (PDF) | https://www.accessdata.fda.gov/drugsatfda_docs/label/2013/021908s011lbl.pdf | |
11/26/2012 | SUPPL-10 | Labeling-Package Insert | Label (PDF) | https://www.accessdata.fda.gov/drugsatfda_docs/label/2012/021908s010lbl.pdf | |
02/24/2011 | SUPPL-8 | Labeling | Label (PDF) | https://www.accessdata.fda.gov/drugsatfda_docs/label/2011/021908s008lbl.pdf | |
04/29/2008 | SUPPL-5 | Efficacy-New Indication | Label (PDF) | https://www.accessdata.fda.gov/drugsatfda_docs/label/2008/021908s005lbl.pdf | |
05/16/2007 | SUPPL-4 | Labeling | Label (PDF) | https://www.accessdata.fda.gov/drugsatfda_docs/label/2007/021908s004lbl.pdf | |
01/31/2006 | ORIG-1 | Approval | Label (PDF) | https://www.accessdata.fda.gov/drugsatfda_docs/label/2006/021908s000lbl.pdf |
AMITIZA
CAPSULE;ORAL; 24MCG
TE Code = AB
Drug Name | Active Ingredients | Strength | Dosage Form/Route | Marketing Status | RLD | TE Code | Application No. | Company |
---|---|---|---|---|---|---|---|---|
AMITIZA | LUBIPROSTONE | 24MCG | CAPSULE;ORAL | Prescription | Yes | AB | 021908 | SUCAMPO PHARMA LLC |
LUBIPROSTONE | LUBIPROSTONE | 24MCG | CAPSULE;ORAL | Prescription | No | AB | 209450 | AMNEAL |
LUBIPROSTONE | LUBIPROSTONE | 24MCG | CAPSULE;ORAL | Prescription | No | AB | 218640 | ASCENT PHARMS INC |
LUBIPROSTONE | LUBIPROSTONE | 24MCG | CAPSULE;ORAL | Prescription | No | AB | 206994 | DR REDDYS |
LUBIPROSTONE | LUBIPROSTONE | 24MCG | CAPSULE;ORAL | Prescription | No | AB | 209920 | TEVA PHARMS USA INC |
LUBIPROSTONE | LUBIPROSTONE | 24MCG | CAPSULE;ORAL | Prescription | No | AB | 214131 | ZYDUS PHARMS |
CAPSULE;ORAL; 8MCG
TE Code = AB
Drug Name | Active Ingredients | Strength | Dosage Form/Route | Marketing Status | RLD | TE Code | Application No. | Company |
---|---|---|---|---|---|---|---|---|
AMITIZA | LUBIPROSTONE | 8MCG | CAPSULE;ORAL | Prescription | Yes | AB | 021908 | SUCAMPO PHARMA LLC |
LUBIPROSTONE | LUBIPROSTONE | 8MCG | CAPSULE;ORAL | Prescription | No | AB | 209450 | AMNEAL |
LUBIPROSTONE | LUBIPROSTONE | 8MCG | CAPSULE;ORAL | Prescription | No | AB | 218640 | ASCENT PHARMS INC |
LUBIPROSTONE | LUBIPROSTONE | 8MCG | CAPSULE;ORAL | Prescription | No | AB | 206994 | DR REDDYS |
LUBIPROSTONE | LUBIPROSTONE | 8MCG | CAPSULE;ORAL | Prescription | No | AB | 209920 | TEVA PHARMS USA INC |
LUBIPROSTONE | LUBIPROSTONE | 8MCG | CAPSULE;ORAL | Prescription | No | AB | 214131 | ZYDUS PHARMS |