Rescula - 17350-015-05 - (Unoprostone Isopropyl)

Alphabetical Index


Drug Information of Rescula

Product NDC: 17350-015
Proprietary Name: Rescula
Non Proprietary Name: Unoprostone Isopropyl
Active Ingredient(s): 1.5    mg/mL & nbsp;   Unoprostone Isopropyl
Administration Route(s): OPHTHALMIC
Dosage Form(s): SOLUTION/ DROPS
Coding System: National Drug Codes(NDC)

Labeler Information of Rescula

Product NDC: 17350-015
Labeler Name: Sucampo Pharma Americas, LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021214
Marketing Category: NDA
Start Marketing Date: 20130107

Package Information of Rescula

Package NDC: 17350-015-05
Package Description: 5 mL in 1 BOTTLE, DROPPER (17350-015-05)

NDC Information of Rescula

NDC Code 17350-015-05
Proprietary Name Rescula
Package Description 5 mL in 1 BOTTLE, DROPPER (17350-015-05)
Product NDC 17350-015
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Unoprostone Isopropyl
Dosage Form Name SOLUTION/ DROPS
Route Name OPHTHALMIC
Start Marketing Date 20130107
Marketing Category Name NDA
Labeler Name Sucampo Pharma Americas, LLC
Substance Name UNOPROSTONE ISOPROPYL
Strength Number 1.5
Strength Unit mg/mL
Pharmaceutical Classes Prostaglandin Analog [EPC],Prostaglandins [Chemical/Ingredient]

Complete Information of Rescula


General Information