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