Details for New Drug Application (NDA): 020886
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The generic ingredient in PANRETIN is alitretinoin. There are two drug master file entries for this compound. One supplier is listed for this compound. Additional details are available on the alitretinoin profile page.
Summary for 020886
Tradename: | PANRETIN |
Applicant: | Concordia |
Ingredient: | alitretinoin |
Patents: | 0 |
Formulation / Manufacturing: | see details |
Suppliers and Packaging for NDA: 020886
Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
---|---|---|---|---|---|---|---|---|
PANRETIN | alitretinoin | GEL;TOPICAL | 020886 | NDA | Concordia Pharmaceuticals Inc. | 59212-601 | 59212-601-22 | 60 g in 1 TUBE (59212-601-22) |
Profile for product number 001
Active Rx/OTC/Discontinued: | RX | Dosage: | GEL;TOPICAL | Strength | EQ 0.1% BASE | ||||
Approval Date: | Feb 2, 1999 | TE: | RLD: | Yes |
Expired US Patents for NDA 020886
Applicant | Tradename | Generic Name | Dosage | NDA | Approval Date | Patent No. | Patent Expiration |
---|---|---|---|---|---|---|---|
Concordia | PANRETIN | alitretinoin | GEL;TOPICAL | 020886-001 | Feb 2, 1999 | ⤷ Sign Up | ⤷ Sign Up |
Concordia | PANRETIN | alitretinoin | GEL;TOPICAL | 020886-001 | Feb 2, 1999 | ⤷ Sign Up | ⤷ Sign Up |
>Applicant | >Tradename | >Generic Name | >Dosage | >NDA | >Approval Date | >Patent No. | >Patent Expiration |
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