Desmopressin Acetate

Product NDC: 47335-788
11-digit product format: 473350788
Labeler code: 47335
Product ID: 47335-788_df0d31d9-48f9-408d-9a97-58d8f9f97a0a
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: Desmopressin Acetate
Dosage form: SOLUTION
Route: NASAL
Labeler: Sun Pharmaceutical Industries, Inc.
Application: ANDA078271
Marketing category: ANDA
Marketing start: 2013-12-24
Marketing end: 0000-00-00
Substance: DESMOPRESSIN ACETATE
Active strength: 0 mg/mL
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
47335-788-91	ML - Milliliter	47335-788	7f81f9ea-0417-422b-b361-24a120761277	1	2014-05-02

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
47335-788-91	47335078891	1 BOTTLE, SPRAY in 1 CARTON (47335-788-91) > 5 mL in 1 BOTTLE, SPRAY	2013-12-24	0000-00-00	No	No	Current