Yosprala is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by Nucare Pharmaceuticals,inc.. The primary component is Aspirin; Omeprazole.
Product ID | 68071-5102_96da6be5-756e-6b0e-e053-2a95a90a9071 |
NDC | 68071-5102 |
Product Type | Human Prescription Drug |
Proprietary Name | Yosprala |
Generic Name | Yosprala |
Dosage Form | Tablet, Film Coated |
Route of Administration | ORAL |
Marketing Start Date | 2019-07-17 |
Marketing Category | NDA / NDA |
Application Number | NDA205103 |
Labeler Name | NuCare Pharmaceuticals,Inc. |
Substance Name | ASPIRIN; OMEPRAZOLE |
Active Ingredient Strength | 81 mg/1; mg/1 |
Pharm Classes | Platelet Aggregation Inhibitor [EPC],Decreased Platelet Aggregation [PE],Cyclooxygenase Inhibitors [MoA],Decreased Prostaglandin Production [PE],Anti-Inflammatory Agents, Non-Steroidal [CS],Nonsteroidal Anti-inflammatory Drug [EPC],Proton Pump Inhibitor [EPC],Proton Pump Inhibitors [MoA],Cytochrome P450 2C19 Inhibitors [MoA] |
NDC Exclude Flag | N |
Listing Certified Through | 2020-12-31 |
Marketing Start Date | 2019-11-08 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | NDA |
Application Number | NDA205103 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2019-11-08 |
Ingredient | Strength |
---|---|
ASPIRIN | 81 mg/1 |
NDC | Brand Name | Generic Name |
---|---|---|
64950-424 | Yosprala | aspirin and omeprazole |
64950-425 | Yosprala | aspirin and omeprazole |
68071-5102 | Yosprala | Yosprala |
70347-081 | YOSPRALA | Aspirin and Omeprazole |
70347-325 | YOSPRALA | Aspirin and Omeprazole |
71800-012 | Yosprala | aspirin and omeprazole |
71800-016 | Yosprala | aspirin and omeprazole |
73568-004 | Yosprala | aspirin and omeprazole |
73568-005 | Yosprala | aspirin and omeprazole |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
YOSPRALA 87107388 not registered Dead/Abandoned |
POZEN Inc 2016-07-18 |
YOSPRALA 86011803 5124592 Live/Registered |
POZEN Inc. 2013-07-16 |