Clomipramine Hydrochloride

Product NDC
70710-1067
11-digit product format
707101067
Labeler code
70710
Product ID
70710-1067_a988ebbb-6e0c-43ff-83a8-0cc0dc4259ce
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Clomipramine Hydrochloride
Dosage form
CAPSULE
Route
ORAL
Labeler
Zydus Pharmaceuticals USA Inc.
Application
ANDA208961
Marketing category
ANDA
Marketing start
2018-05-03
Marketing end
0000-00-00
Substance
CLOMIPRAMINE HYDROCHLORIDE
Active strength
75 mg/1
Pharmacologic classes
Tricyclic Antidepressant [EPC]
NDC exclude flag
No
Listing certified through
2023-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
70710-1067-1EA - Each70710-1067427bd5db-1bf8-4398-bedb-83489e7d3eee12018-08-13
70710-1067-3EA - Each70710-10678079f5bb-20ad-44f9-a6aa-de32bc2d5a1c12018-08-13

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
70710-1067-170710106701100 CAPSULE in 1 BOTTLE (70710-1067-1) 100 capsule2018-05-030000-00-00NoNoCurrent
70710-1067-37071010670330 CAPSULE in 1 BOTTLE (70710-1067-3) 30 capsule2018-05-030000-00-00NoNoCurrent
70710-1067-97071010670990 CAPSULE in 1 BOTTLE (70710-1067-9) 90 capsule2018-05-030000-00-00NoNoCurrent