Desmopressin Acetate

Product NDC: 68001-326
11-digit product format: 680010326
Labeler code: 68001
Product ID: 68001-326_99d6876c-a651-73ce-e053-2995a90a7866
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: Desmopressin Acetate
Dosage form: TABLET
Route: ORAL
Labeler: BluePoint Laboratories
Application: ANDA201831
Marketing category: ANDA
Marketing start: 2017-04-30
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
68001-326-00	EA - Each	68001-326	9a54954e-7e3f-4d62-a41a-708acd6b16aa	1	2017-07-07

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
68001-326-00	68001032600	100 TABLET in 1 BOTTLE (68001-326-00)	100 tablet	2017-04-30	0000-00-00	No	No	Current