Desmopressin Acetate

Product NDC: 16714-884
11-digit product format: 167140884
Labeler code: 16714
Product ID: 16714-884_70b95626-59a2-4552-84e1-f0063ee9c452
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: Desmopressin Acetate
Dosage form: TABLET
Route: ORAL
Labeler: Northstar Rx LLC
Application: ANDA201831
Marketing category: ANDA
Marketing start: 2015-05-28
Marketing end: 0000-00-00
Substance: DESMOPRESSIN ACETATE
Active strength: 0 mg/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: 2020-12-31
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
16714-884-01	EA - Each	16714-884	4404307d-6f49-4b6d-96b9-c650b991de87	1	2019-04-11

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
16714-884-01	16714088401	100 TABLET in 1 BOTTLE (16714-884-01)	100 tablet	2018-12-31	0000-00-00	No	No	Current