Desmopressin Acetate

Product NDC: 68001-234
11-digit product format: 680010234
Labeler code: 68001
Product ID: 68001-234_99096fc1-cdb2-3f16-e053-2a95a90a652b
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: Desmopressin Acetate
Dosage form: TABLET
Route: ORAL
Labeler: BluePoint Laboratories
Application: ANDA076470
Marketing category: ANDA
Marketing start: 2014-02-27
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
68001-234-00	EA - Each	68001-234	0ee894d3-748c-4e7f-bbd8-a1305c07cbeb	1	2014-04-03

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
68001-234-00	68001023400	100 TABLET in 1 BOTTLE, PLASTIC (68001-234-00)	100 tablet	2014-02-27	0000-00-00	No	No	Current