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"55700-505-30" National Drug Code (NDC)
Duloxetine 30 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (55700-505-30)
(Lake Erie Medical DBA Quality Care Products LLC)
NDC Code
55700-505-30
Package Description
30 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (55700-505-30)
Product NDC
55700-505
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Duloxetine
Proprietary Name Suffix
Delayed-release
Non-Proprietary Name
Duloxetine Hydrochloride
Dosage Form
CAPSULE, DELAYED RELEASE PELLETS
Usage
ORAL
Start Marketing Date
20140611
Marketing Category Name
ANDA
Application Number
ANDA203088
Manufacturer
Lake Erie Medical DBA Quality Care Products LLC
Substance Name
DULOXETINE HYDROCHLORIDE
Strength
30
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/55700-505-30