Desmopressin Acetate

Product NDC: 69918-501
11-digit product format: 699180501
Labeler code: 69918
Product ID: 69918-501_5cca6c70-48ee-42ed-b0dc-5e61f7164541
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: Desmopressin Acetate
Dosage form: SPRAY
Route: NASAL
Labeler: Amring Pharmaceuticals, Inc.
Application: NDA017922
Marketing category: NDA AUTHORIZED GENERIC
Marketing start: 2016-04-06
Marketing end: 2022-05-31
Substance: DESMOPRESSIN ACETATE
Active strength: 10 ug/.1mL
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: 0000-00-00
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
69918-501-05	ML - Milliliter	69918-501	362a15ea-df23-4558-ac41-0c48a06aaa9a	1	2016-05-16

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	Marketing start	Marketing end	Sample	Exclude flag	Status
69918-501-05	69918050105	1 BOTTLE, SPRAY in 1 CARTON (69918-501-05) > 5 mL in 1 BOTTLE, SPRAY	2016-04-06	2022-05-31	No	No	Current