NOCDURNA is a Sublingual Tablet in the Human Prescription Drug category. It is labeled and distributed by Ferring Pharmaceuticals Inc.. The primary component is Desmopressin Acetate.
Product ID | 55566-5070_763a3d42-80dc-491a-b67d-7098d8cafb0b |
NDC | 55566-5070 |
Product Type | Human Prescription Drug |
Proprietary Name | NOCDURNA |
Generic Name | Desmopressin Acetate |
Dosage Form | Tablet |
Route of Administration | SUBLINGUAL |
Marketing Start Date | 2018-10-22 |
Marketing Category | NDA / NDA |
Application Number | NDA022517 |
Labeler Name | Ferring Pharmaceuticals Inc. |
Substance Name | DESMOPRESSIN ACETATE |
Active Ingredient Strength | 55 ug/1 |
Pharm Classes | Factor VIII Activator [EPC],Increased Coagulation Factor VIII Activity [PE],Increased Coagulation Factor VIII Concentration [PE],Vasopressin Analog [EPC],Vasopressins [CS] |
NDC Exclude Flag | N |
Listing Certified Through | 2022-12-31 |
Marketing Start Date | 2018-10-22 |
Marketing End Date | 2023-02-28 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | NDA |
Application Number | NDA022517 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2018-06-29 |
Marketing Category | NDA |
Application Number | NDA022517 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2018-06-29 |
Ingredient | Strength |
---|---|
DESMOPRESSIN ACETATE | 55.3 ug/1 |
SPL SET ID: | 8ef937d4-0bb5-46bd-9b53-9b14b9d2738f |
Manufacturer | |
UNII | |
RxNorm Concept Unique ID - RxCUI |
NDC | Brand Name | Generic Name |
---|---|---|
54436-325 | NOCDURNA | DESMOPRESSIN ACETATE |
55566-5050 | NOCDURNA | NOCDURNA |
55566-5070 | NOCDURNA | NOCDURNA |
0115-1646 | Desmopressin Acetate | Desmopressin Acetate |
0115-1647 | Desmopressin Acetate | Desmopressin Acetate |
0409-2265 | Desmopressin Acetate | Desmopressin Acetate |
0517-4310 | Desmopressin Acetate | Desmopressin Acetate |
0591-2464 | Desmopressin Acetate | Desmopressin Acetate |
0591-2465 | Desmopressin Acetate | Desmopressin Acetate |
0615-7549 | Desmopressin Acetate | Desmopressin Acetate |
0703-5051 | Desmopressin acetate | Desmopressin acetate |
0703-5054 | Desmopressin acetate | Desmopressin acetate |
10702-169 | Desmopressin Acetate | Desmopressin Acetate |
10702-170 | Desmopressin Acetate | Desmopressin Acetate |
16714-015 | Desmopressin Acetate | Desmopressin Acetate |
16714-883 | Desmopressin Acetate | Desmopressin Acetate |
16714-884 | Desmopressin Acetate | Desmopressin Acetate |
23155-489 | Desmopressin Acetate | Desmopressin Acetate |
23155-490 | Desmopressin Acetate | Desmopressin Acetate |
24208-342 | Desmopressin Acetate | Desmopressin Acetate |
25021-460 | desmopressin acetate | desmopressin acetate |
25021-461 | desmopressin acetate | desmopressin acetate |
43598-053 | Desmopressin Acetate | Desmopressin Acetate |
43598-931 | DESMOPRESSIN ACETATE | DESMOPRESSIN ACETATE |
47335-788 | Desmopressin Acetate | Desmopressin Acetate |
50268-220 | Desmopressin Acetate | Desmopressin Acetate |
50268-221 | Desmopressin Acetate | Desmopressin Acetate |
0053-6871 | Stimate | DESMOPRESSIN ACETATE |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
NOCDURNA 76698840 4405021 Live/Registered |
Ferring B.V. 2009-08-07 |