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"0781-1972-01" National Drug Code (NDC)
Desipramine Hydrochloride 100 TABLET, FILM COATED in 1 BOTTLE (0781-1972-01)
(Sandoz Inc)
NDC Code
0781-1972-01
Package Description
100 TABLET, FILM COATED in 1 BOTTLE (0781-1972-01)
Product NDC
0781-1972
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Desipramine Hydrochloride
Non-Proprietary Name
Desipramine Hydrochloride
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
19880524
End Marketing Date
20200630
Marketing Category Name
ANDA
Application Number
ANDA072100
Manufacturer
Sandoz Inc
Substance Name
DESIPRAMINE HYDROCHLORIDE
Strength
25
Strength Unit
mg/1
Pharmacy Classes
Tricyclic Antidepressant [EPC]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/0781-1972-01