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"0781-2822-10" National Drug Code (NDC)
Fluoxetine Hydrochloride 1000 CAPSULE in 1 BOTTLE (0781-2822-10)
(Sandoz Inc)
NDC Code
0781-2822-10
Package Description
1000 CAPSULE in 1 BOTTLE (0781-2822-10)
Product NDC
0781-2822
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Fluoxetine Hydrochloride
Non-Proprietary Name
Fluoxetine Hydrochloride
Dosage Form
CAPSULE
Usage
ORAL
Start Marketing Date
20020129
End Marketing Date
20221031
Marketing Category Name
ANDA
Application Number
ANDA075049
Manufacturer
Sandoz Inc
Substance Name
FLUOXETINE HYDROCHLORIDE
Strength
20
Strength Unit
mg/1
Pharmacy Classes
Serotonin Reuptake Inhibitor [EPC], Serotonin Uptake Inhibitors [MoA]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/0781-2822-10