Desipramine Hydrochloride

Product NDC
68151-2482
11-digit product format
681512482
Labeler code
68151
Product ID
68151-2482_986b6865-dfd4-4982-853f-80be12651b20
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Desipramine Hydrochloride
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Carilion Materials Management
Application
ANDA072099
Marketing category
ANDA
Marketing start
1988-05-24
Marketing end
0000-00-00
Substance
DESIPRAMINE HYDROCHLORIDE
Active strength
10 mg/1
Pharmacologic classes
Tricyclic Antidepressant [EPC]
NDC exclude flag
E
Listing certified through
2018-12-31
Current FDA listing
Historical FDA.report record

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
bda46dda-4ebd-3e63-0043-123c9d173af2Product name620220125

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
68151-2482-02020-01-31C16284748780-19d75b9d0-1888-f424-e053-dadaa90a57ceDesipramine Hydrochloride Tablets, USP

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
68151-2482-0Desipramine Hydrochloride1 in 1 PACKAGETABLET, FILM COATED16

DailyMed Socrata Ingredients#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
68151-2482DESIPRAMINE HYDROCHLORIDE TABLET, FILM COATED [CARILION MATERIALS MANAGEMENT]6Legacy NDC, 1 package rows20171228_b5e9fa99-e2dd-4271-8bd4-ea865b6ddb48.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
1099288desipramine HCl 10 MG Oral TabletPSNb5e9fa99-e2dd-4271-8bd4-ea865b6ddb486
1099288desipramine hydrochloride 10 MG Oral TabletSCDb5e9fa99-e2dd-4271-8bd4-ea865b6ddb486

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionStatus
68151-2482-0681512482001 in 1 PACKAGEHistorical