FDA.reportPublic FDA data

IMIPRAMINE HYDROCHLORIDE

Product NDC
51655-455
11-digit product format
516550455
Labeler code
51655
Product ID
51655-455_e7c5e5ad-85f5-41c5-bb05-33890e8c07be
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
IMIPRAMINE HYDROCHLORIDE
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Northwind Pharmaceuticals, LLC
Application
ANDA084937
Marketing category
ANDA
Marketing start
2015-03-06
Marketing end
0000-00-00
Substance
IMIPRAMINE HYDROCHLORIDE
Active strength
50 mg/1
Pharmacologic classes
Tricyclic Antidepressant [EPC]
NDC exclude flag
No
Listing certified through
2019-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
51655-455-832026-01-07C16284748780-19d75b9d1-0a14-f424-e053-dadaa90a57cefa959867-4c35-4c23-8ac7-2380f3b251ec
51655-455-832020-01-31C16284748780-19d75b9d1-0a14-f424-e053-dadaa90a57cefa959867-4c35-4c23-8ac7-2380f3b251ec

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
IMIPRAMINE HYDROCHLORIDEACTIVE INGREDIENTBKE5Q1J60UIMIPRAMINE HYDROCHLORIDE TABLET, FILM COATED [NORTHWIND PHARMACEUTICALS, LLC]1
IMIPRAMINEACTIVE MOIETYOGG85SX4E4IMIPRAMINE HYDROCHLORIDE TABLET, FILM COATED [NORTHWIND PHARMACEUTICALS, LLC]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
51655-455IMIPRAMINE HYDROCHLORIDE TABLET, FILM COATED [NORTHWIND PHARMACEUTICALS, LLC]1Legacy NDC20150323_fa959867-4c35-4c23-8ac7-2380f3b251ec.zip