Drugs@FDA: FDA-Approved Drugs
New Drug Application (NDA): 019599
Company: LEGACY PHARMA
Company: LEGACY PHARMA
Drug Name | Active Ingredients | Strength | Dosage Form/Route | Marketing Status | TE Code | RLD | RS |
---|---|---|---|---|---|---|---|
NAFTIN | NAFTIFINE HYDROCHLORIDE | 1% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | CREAM;TOPICAL | Discontinued | None | Yes | No |
NAFTIN | NAFTIFINE HYDROCHLORIDE | 2% | CREAM;TOPICAL | Prescription | AB | Yes | Yes |
Original Approvals or Tentative Approvals
Action Date | Submission | Action Type | Submission Classification | Review Priority; Orphan Status | Letters, Reviews, Labels, Patient Package Insert | Notes | Url |
---|---|---|---|---|---|---|---|
02/29/1988 | ORIG-1 | Approval | Type 1 - New Molecular Entity | 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 |
---|---|---|---|---|---|
04/30/2018 | SUPPL-14 | Labeling-Package Insert |
Label (PDF)
Letter (PDF) |
https://www.accessdata.fda.gov/drugsatfda_docs/label/2018/019356s008,019599s014,204286s003lbl.pdf https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2018/019356Orig1s008,019599Orig1s014,204286Orig1s003ltr.pdf | |
11/10/2016 | SUPPL-13 | Efficacy-New Patient Population |
Label (PDF)
Letter (PDF) |
https://www.accessdata.fda.gov/drugsatfda_docs/label/2016/019599s013lbl.pdf https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2016/019599Orig1s013ltr.pdf | |
10/10/2014 | SUPPL-12 | Efficacy-New Patient Population |
Label (PDF)
Letter (PDF) |
https://www.accessdata.fda.gov/drugsatfda_docs/label/2014/019599s012lbledt.pdf https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2014/019599Orig1s012ltr.pdf | |
01/13/2012 | SUPPL-11 | Efficacy-New Dosing Regimen |
Label (PDF)
Letter (PDF) Review (PDF) |
https://www.accessdata.fda.gov/drugsatfda_docs/label/2012/019599s011lbl.pdf https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2012/019599s011ltr.pdf https://www.accessdata.fda.gov/drugsatfda_docs/nda/2012/019599Orig1s011.pdf | |
01/26/2009 | SUPPL-10 | Labeling-Package Insert |
Letter (PDF)
|
Label is not available on this site. |
https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2009/019599s010ltr.pdf |
08/10/2006 | SUPPL-9 | Labeling-Container/Carton Labels, Labeling-Package Insert |
Label is not available on this site. |
||
06/04/2002 | SUPPL-7 | Manufacturing (CMC) |
Review (PDF)
|
Label is not available on this site. |
https://www.accessdata.fda.gov/drugsatfda_docs/nda/2002/019599Orig1s007.pdf |
11/30/1998 | SUPPL-6 | Manufacturing (CMC) |
Label is not available on this site. |
||
09/24/1997 | SUPPL-5 | Manufacturing (CMC)-Control |
Label is not available on this site. |
||
06/15/1995 | SUPPL-4 | Manufacturing (CMC)-Packaging |
Label is not available on this site. |
||
01/30/1990 | SUPPL-3 | Manufacturing (CMC)-Control |
Label is not available on this site. |
||
07/05/1990 | SUPPL-2 | Efficacy-New Dosing Regimen |
Label is not available on this site. |
||
04/05/1989 | SUPPL-1 | Efficacy-New Indication |
Label is not available on this site. |
Action Date | Submission | Supplement Categories or Approval Type | Letters, Reviews, Labels, Patient Package Insert |
Note | Url |
---|---|---|---|---|---|
04/30/2018 | SUPPL-14 | Labeling-Package Insert | Label (PDF) | https://www.accessdata.fda.gov/drugsatfda_docs/label/2018/019356s008,019599s014,204286s003lbl.pdf | |
11/10/2016 | SUPPL-13 | Efficacy-New Patient Population | Label (PDF) | https://www.accessdata.fda.gov/drugsatfda_docs/label/2016/019599s013lbl.pdf | |
10/10/2014 | SUPPL-12 | Efficacy-New Patient Population | Label (PDF) | https://www.accessdata.fda.gov/drugsatfda_docs/label/2014/019599s012lbledt.pdf | |
01/13/2012 | SUPPL-11 | Efficacy-New Dosing Regimen | Label (PDF) | https://www.accessdata.fda.gov/drugsatfda_docs/label/2012/019599s011lbl.pdf |
NAFTIN
CREAM;TOPICAL; 2%
TE Code = AB
Drug Name | Active Ingredients | Strength | Dosage Form/Route | Marketing Status | RLD | TE Code | Application No. | Company |
---|---|---|---|---|---|---|---|---|
NAFTIFINE HYDROCHLORIDE | NAFTIFINE HYDROCHLORIDE | 2% | CREAM;TOPICAL | Prescription | No | AB | 206960 | AMNEAL |
NAFTIFINE HYDROCHLORIDE | NAFTIFINE HYDROCHLORIDE | 2% | CREAM;TOPICAL | Prescription | No | AB | 206901 | TARO |
NAFTIFINE HYDROCHLORIDE | NAFTIFINE HYDROCHLORIDE | 2% | CREAM;TOPICAL | Prescription | No | AB | 210038 | XIROMED |
NAFTIN | NAFTIFINE HYDROCHLORIDE | 2% | CREAM;TOPICAL | Prescription | Yes | AB | 019599 | LEGACY PHARMA |