REFISSA - 66530-411-05 - (TRETINOIN)

Alphabetical Index


Drug Information of REFISSA

Product NDC: 66530-411
Proprietary Name: REFISSA
Non Proprietary Name: TRETINOIN
Active Ingredient(s): .5    mg/g & nbsp;   TRETINOIN
Administration Route(s): TOPICAL
Dosage Form(s): CREAM
Coding System: National Drug Codes(NDC)

Labeler Information of REFISSA

Product NDC: 66530-411
Labeler Name: Spear Dermatology Products
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076498
Marketing Category: ANDA
Start Marketing Date: 20090617

Package Information of REFISSA

Package NDC: 66530-411-05
Package Description: 5 g in 1 TUBE (66530-411-05)

NDC Information of REFISSA

NDC Code 66530-411-05
Proprietary Name REFISSA
Package Description 5 g in 1 TUBE (66530-411-05)
Product NDC 66530-411
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name TRETINOIN
Dosage Form Name CREAM
Route Name TOPICAL
Start Marketing Date 20090617
Marketing Category Name ANDA
Labeler Name Spear Dermatology Products
Substance Name TRETINOIN
Strength Number .5
Strength Unit mg/g
Pharmaceutical Classes Retinoid [EPC],Retinoids [Chemical/Ingredient]

Complete Information of REFISSA


General Information