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"0781-1396-10" National Drug Code (NDC)
Haloperidol 1000 TABLET in 1 BOTTLE (0781-1396-10)
(Sandoz Inc)
NDC Code
0781-1396-10
Package Description
1000 TABLET in 1 BOTTLE (0781-1396-10)
Product NDC
0781-1396
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Haloperidol
Non-Proprietary Name
Haloperidol
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
19861117
End Marketing Date
20201231
Marketing Category Name
ANDA
Application Number
ANDA071209
Manufacturer
Sandoz Inc
Substance Name
HALOPERIDOL
Strength
5
Strength Unit
mg/1
Pharmacy Classes
Typical Antipsychotic [EPC]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/0781-1396-10