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"57237-018-99" National Drug Code (NDC)
Duloxetine 1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (57237-018-99)
(Rising Pharma Holdings, Inc.)
NDC Code
57237-018-99
Package Description
1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (57237-018-99)
Product NDC
57237-018
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Duloxetine
Non-Proprietary Name
Duloxetine Hydrochloride
Dosage Form
CAPSULE, DELAYED RELEASE
Usage
ORAL
Start Marketing Date
20131211
Marketing Category Name
ANDA
Application Number
ANDA090778
Manufacturer
Rising Pharma Holdings, Inc.
Substance Name
DULOXETINE HYDROCHLORIDE
Strength
30
Strength Unit
mg/1
Pharmacy Classes
Norepinephrine Uptake Inhibitors [MoA], Serotonin Uptake Inhibitors [MoA], Serotonin and Norepinephrine Reuptake Inhibitor [EPC]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/57237-018-99