Myorisan - 61748-304-11 - (isotretinoin)

Alphabetical Index


Drug Information of Myorisan

Product NDC: 61748-304
Proprietary Name: Myorisan
Non Proprietary Name: isotretinoin
Active Ingredient(s): 40    mg/1 & nbsp;   isotretinoin
Administration Route(s): ORAL
Dosage Form(s): CAPSULE, LIQUID FILLED
Coding System: National Drug Codes(NDC)

Labeler Information of Myorisan

Product NDC: 61748-304
Labeler Name: VersaPharm Incorporated
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076485
Marketing Category: ANDA
Start Marketing Date: 20120501

Package Information of Myorisan

Package NDC: 61748-304-11
Package Description: 10 BLISTER PACK in 1 CARTON (61748-304-11) > 10 CAPSULE, LIQUID FILLED in 1 BLISTER PACK

NDC Information of Myorisan

NDC Code 61748-304-11
Proprietary Name Myorisan
Package Description 10 BLISTER PACK in 1 CARTON (61748-304-11) > 10 CAPSULE, LIQUID FILLED in 1 BLISTER PACK
Product NDC 61748-304
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name isotretinoin
Dosage Form Name CAPSULE, LIQUID FILLED
Route Name ORAL
Start Marketing Date 20120501
Marketing Category Name ANDA
Labeler Name VersaPharm Incorporated
Substance Name ISOTRETINOIN
Strength Number 40
Strength Unit mg/1
Pharmaceutical Classes Retinoid [EPC],Retinoids [Chemical/Ingredient]

Complete Information of Myorisan


General Information