NDC 53436-084
VELTASSA
Patiromer
VELTASSA is a Oral Powder, For Suspension in the Human Prescription Drug category. It is labeled and distributed by Vifor Pharma, Inc.. The primary component is Patiromer.
| Product ID | 53436-084_0259a872-3b9a-445c-8dc4-86f6aadf129a |
| NDC | 53436-084 |
| Product Type | Human Prescription Drug |
| Proprietary Name | VELTASSA |
| Generic Name | Patiromer |
| Dosage Form | Powder, For Suspension |
| Route of Administration | ORAL |
| Marketing Start Date | 2015-10-23 |
| Marketing Category | NDA / NDA |
| Application Number | NDA205739 |
| Labeler Name | Vifor Pharma, Inc. |
| Substance Name | PATIROMER |
| Active Ingredient Strength | 8 g/1 |
| Pharm Classes | Potassium Binder [EPC],Potassium Ion Binding Activity [MoA] |
| NDC Exclude Flag | N |
| Listing Certified Through | 2022-12-31 |
Packaging
NDC 53436-084-04
4 PACKET in 1 CARTON (53436-084-04) > 1 POWDER, FOR SUSPENSION in 1 PACKET (53436-084-01)
| Marketing Start Date | 2015-10-23 |
| NDC Exclude Flag | N |
| Sample Package? | N |
NDC SPL Data Element Entries
NDC 53436-084-92 [53436008492]
VELTASSA POWDER, FOR SUSPENSION
| Marketing Category | NDA |
| Application Number | NDA205739 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2016-05-01 |
NDC 53436-084-04 [53436008404]
VELTASSA POWDER, FOR SUSPENSION
| Marketing Category | NDA |
| Application Number | NDA205739 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2015-10-23 |
NDC 53436-084-91 [53436008491]
VELTASSA POWDER, FOR SUSPENSION
| Marketing Category | NDA |
| Application Number | NDA205739 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2016-05-01 |
NDC 53436-084-30 [53436008430]
VELTASSA POWDER, FOR SUSPENSION
| Marketing Category | NDA |
| Application Number | NDA205739 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2015-10-23 |
NDC 53436-084-01 [53436008401]
VELTASSA POWDER, FOR SUSPENSION
| Marketing Category | NDA |
| Application Number | NDA205739 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2015-10-23 |
Drug Details
Active Ingredients
| Ingredient | Strength |
|---|---|
| PATIROMER | 8.4 g/1 |
OpenFDA Data
| SPL SET ID: | bf002984-d6c9-46df-aecb-a07733f763c1 |
| Manufacturer | |
| UNII | |
| RxNorm Concept Unique ID - RxCUI |
Pharmacological Class
- Potassium Binder [EPC]
- Potassium Ion Binding Activity [MoA]
Medicade Reported Pricing
53436008430 VELTASSA 8.4 GM POWDER PACKET
Pricing Unit: EA | Drug Type:
53436008404 VELTASSA 8.4 GM POWDER PACKET
Pricing Unit: EA | Drug Type:
53436008401 VELTASSA 8.4 GM POWDER PACKET
Pricing Unit: EA | Drug Type:
NDC Crossover Matching brand name "VELTASSA" or generic name "Patiromer"
| NDC | Brand Name | Generic Name |
|---|---|---|
| 53436-084 | VELTASSA | patiromer |
| 53436-168 | VELTASSA | patiromer |
| 53436-252 | VELTASSA | patiromer |
Trademark Results [VELTASSA]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 VELTASSA 86235807 4933010 Live/Registered |
Relypsa, Inc. 2014-03-28 |
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