Desipramine Hydrochloride

Product NDC
64720-416
11-digit product format
647200416
Labeler code
64720
Product ID
64720-416_44fdecf5-ad29-4abc-a7f9-7a5e7e4f0f9b
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
desipramine hydrochloride
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
CorePharma, LLC
Application
ANDA205153
Marketing category
ANDA
Marketing start
2017-07-14
Marketing end
2019-09-30
Substance
DESIPRAMINE HYDROCHLORIDE
Active strength
25 mg/1
Pharmacologic classes
Tricyclic Antidepressant [EPC]
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 NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
64720-416-10EA - Each64720-4166fe5df37-588a-4012-9932-61b8a79576a812017-08-11