Desipramine Hydrochloride

Product NDC
0781-1972
11-digit product format
007811972
Labeler code
0781
Product ID
0781-1972_69485d1b-0164-4d9b-b3b9-9b29304ab311
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Desipramine Hydrochloride
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Sandoz Inc
Application
ANDA072100
Marketing category
ANDA
Marketing start
1988-05-24
Marketing end
2020-06-30
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 Product Concepts#

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

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0781-1972-01EA - Each0781-1972de1be849-8563-4f0e-8023-e880a19a610c12012-07-24
0781-1972-10EA - Each0781-19723f115a90-c56e-412d-b2cb-2dbd4f449c9312015-10-02

DailyMed Socrata Ingredients#

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
1099300desipramine HCl 25 MG Oral TabletPSNf3127fff-2943-424d-8b8b-80aa320a2d071
1099300desipramine hydrochloride 25 MG Oral TabletSCDf3127fff-2943-424d-8b8b-80aa320a2d071