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"55700-435-30" National Drug Code (NDC)
Duloxetine Hydrochloride 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (55700-435-30)
(Lake Erie Medical DBA Quality Care Products LLC)
NDC Code
55700-435-30
Package Description
30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (55700-435-30)
Product NDC
55700-435
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Duloxetine Hydrochloride
Non-Proprietary Name
Duloxetine Hydrochloride
Dosage Form
CAPSULE, DELAYED RELEASE
Usage
ORAL
Start Marketing Date
20140820
Marketing Category Name
ANDA
Application Number
ANDA202045
Manufacturer
Lake Erie Medical DBA Quality Care Products LLC
Substance Name
DULOXETINE HYDROCHLORIDE
Strength
20
Strength Unit
mg/1
Pharmacy Classes
Norepinephrine Uptake Inhibitors [MoA],Serotonin and Norepinephrine Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/55700-435-30