NOCDURNA

Product NDC: 55566-5070
11-digit product format: 555665070
Labeler code: 55566
Product ID: 55566-5070_763a3d42-80dc-491a-b67d-7098d8cafb0b
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: DESMOPRESSIN ACETATE
Dosage form: TABLET
Route: SUBLINGUAL
Labeler: Ferring Pharmaceuticals Inc.
Application: NDA022517
Marketing category: NDA
Marketing start: 2018-10-22
Marketing end: 0000-00-00
Substance: DESMOPRESSIN ACETATE
Active strength: 55 ug/1
Pharmacologic 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: No
Listing certified through: 2022-12-31
Current FDA listing: Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
55566-5070-1	EA - Each	55566-5070	b3a7b73a-00bc-47e4-b29d-a610f24bfce2	1	2018-11-06

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
XB13HYU18U	DESMOPRESSIN ACETATE	62357-86-2	DESMOPRESSIN ACETATE

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
55566-5070-1	55566507001	3 BLISTER PACK in 1 CARTON (55566-5070-1) > 10 TABLET in 1 BLISTER PACK (55566-5070-0)	3 blister pack	2018-10-22	2023-02-28	No	No	Current