Desipramine Hydrochloride

Product NDC
0781-1975
11-digit product format
007811975
Labeler code
0781
Product ID
0781-1975_69485d1b-0164-4d9b-b3b9-9b29304ab311
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Desipramine Hydrochloride
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Sandoz Inc
Application
ANDA072103
Marketing category
ANDA
Marketing start
1988-06-20
Marketing end
2019-12-31
Substance
DESIPRAMINE HYDROCHLORIDE
Active strength
100 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
0781-1975-01EA - Each0781-19759c6dc299-bc26-4c1d-b2b7-6496a226accc12012-07-24

DailyMed Socrata Ingredients#

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
1099288desipramine HCl 10 MG Oral TabletPSN711d8455-9ce1-45b4-875d-007b2e0b27ec1
1099292desipramine HCl 100 MG Oral TabletPSN711d8455-9ce1-45b4-875d-007b2e0b27ec1
1099288desipramine hydrochloride 10 MG Oral TabletSCD711d8455-9ce1-45b4-875d-007b2e0b27ec1
1099292desipramine hydrochloride 100 MG Oral TabletSCD711d8455-9ce1-45b4-875d-007b2e0b27ec1