Adempas is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by Bayer Healthcare Pharmaceuticals Inc.. The primary component is Riociguat.
| Product ID | 50419-250_12583df4-9db2-4d88-b104-bb49b28e54ff |
| NDC | 50419-250 |
| Product Type | Human Prescription Drug |
| Proprietary Name | Adempas |
| Generic Name | Riociguat |
| Dosage Form | Tablet, Film Coated |
| Route of Administration | ORAL |
| Marketing Start Date | 2013-10-08 |
| Marketing Category | NDA / NDA |
| Application Number | NDA204819 |
| Labeler Name | Bayer HealthCare Pharmaceuticals Inc. |
| Substance Name | RIOCIGUAT |
| Active Ingredient Strength | 1 mg/1 |
| Pharm Classes | Guanylate Cyclase Stimulators [MoA],Soluble Guanylate Cyclase Stimulator [EPC] |
| NDC Exclude Flag | N |
| Listing Certified Through | 2020-12-31 |
| Marketing Start Date | 2013-10-08 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | NDA |
| Application Number | NDA204819 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2013-10-08 |
| Marketing Category | NDA |
| Application Number | NDA204819 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2013-10-08 |
| Marketing Category | NDA |
| Application Number | NDA204819 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2014-09-18 |
| Ingredient | Strength |
|---|---|
| RIOCIGUAT | .5 mg/1 |
| SPL SET ID: | 7b57509a-3d5d-41d4-8fed-1471e26372a3 |
| Manufacturer | |
| UNII | |
| RxNorm Concept Unique ID - RxCUI |
| NDC | Brand Name | Generic Name |
|---|---|---|
| 50419-250 | Adempas | riociguat |
| 50419-251 | Adempas | riociguat |
| 50419-252 | Adempas | riociguat |
| 50419-253 | Adempas | riociguat |
| 50419-254 | Adempas | riociguat |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() ADEMPAS 77723142 3718134 Live/Registered |
Bayer Aktiengesellschaft 2009-04-27 |