NDC 65649-400
Plenvu
Polyethylene Glycol 3350, Sodium Sulfate, Sodium Chloride, Potassium Chloride, Ascorbic Acid, Sodium
Plenvu is a Kit in the Human Prescription Drug category. It is labeled and distributed by Salix Pharmaceuticals, In. The primary component is .
| Product ID | 65649-400_46e1600f-4fd7-4189-9268-2bf48086c855 |
| NDC | 65649-400 |
| Product Type | Human Prescription Drug |
| Proprietary Name | Plenvu |
| Generic Name | Polyethylene Glycol 3350, Sodium Sulfate, Sodium Chloride, Potassium Chloride, Ascorbic Acid, Sodium |
| Dosage Form | Kit |
| Marketing Start Date | 2018-05-04 |
| Marketing Category | NDA / NDA |
| Application Number | NDA209381 |
| Labeler Name | Salix Pharmaceuticals, In |
| Active Ingredient Strength | 0 |
| NDC Exclude Flag | N |
| Listing Certified Through | 2019-12-31 |
Packaging
NDC 65649-400-01
1 KIT in 1 CARTON (65649-400-01) * 46.26 POWDER, FOR SOLUTION in 1 POUCH * 55.65 POWDER, FOR SOLUTION in 1 POUCH * 115.96 POWDER, FOR SOLUTION in 1 POUCH
| Marketing Start Date | 2018-05-04 |
| NDC Exclude Flag | N |
| Sample Package? | N |
NDC SPL Data Element Entries
NDC 65649-400-02 [65649040002]
Plenvu KIT
| Marketing Category | NDA |
| Application Number | NDA209381 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2018-05-04 |
NDC 65649-400-01 [65649040001]
Plenvu KIT
| Marketing Category | NDA |
| Application Number | NDA209381 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2018-05-04 |
Drug Details
OpenFDA Data
| SPL SET ID: | 79f930fa-5674-4f30-8ae8-9448d6243797 |
| Manufacturer | |
| RxNorm Concept Unique ID - RxCUI |
Medicade Reported Pricing
65649040001 PLENVU POWDER PACKETS
Pricing Unit: EA | Drug Type:
Trademark Results [Plenvu]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 PLENVU 79187028 5116648 Live/Registered |
Velinor AG 2016-03-02 |
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