Absorica - 10631-115-31 - (isotretinoin)

Alphabetical Index


Drug Information of Absorica

Product NDC: 10631-115
Proprietary Name: Absorica
Non Proprietary Name: isotretinoin
Active Ingredient(s): 10    mg/1 & nbsp;   isotretinoin
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Absorica

Product NDC: 10631-115
Labeler Name: Ranbaxy Laboratories Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021951
Marketing Category: NDA
Start Marketing Date: 20120608

Package Information of Absorica

Package NDC: 10631-115-31
Package Description: 3 BLISTER PACK in 1 BOX (10631-115-31) > 10 CAPSULE in 1 BLISTER PACK (10631-115-69)

NDC Information of Absorica

NDC Code 10631-115-31
Proprietary Name Absorica
Package Description 3 BLISTER PACK in 1 BOX (10631-115-31) > 10 CAPSULE in 1 BLISTER PACK (10631-115-69)
Product NDC 10631-115
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name isotretinoin
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20120608
Marketing Category Name NDA
Labeler Name Ranbaxy Laboratories Inc.
Substance Name ISOTRETINOIN
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes Retinoid [EPC],Retinoids [Chemical/Ingredient]

Complete Information of Absorica


General Information