Desmopressin acetate

Product NDC: 0703-5054
11-digit product format: 007035054
Labeler code: 0703
Product ID: 0703-5054_85956c95-660a-4d31-a78a-3ee4c379f325
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: Desmopressin acetate
Dosage form: INJECTION
Route: INTRAVENOUS
Labeler: Teva Parenteral Medicines, Inc.
Application: ANDA074888
Marketing category: ANDA
Marketing start: 1997-11-01
Marketing end: 0000-00-00
Substance: DESMOPRESSIN ACETATE
Active strength: 4 ug/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
0703-5054-01	ML - Milliliter	0703-5054	53295b77-e065-4977-820c-1917171af23c	1	2012-07-24

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
0703-5054-01	00703505401	1 VIAL in 1 CARTON (0703-5054-01) > 10 mL in 1 VIAL	1 vial	1997-11-01	0000-00-00	No	No	Current