| 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] |