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"68788-9371-1" National Drug Code (NDC)
Duloxetine Hydrochloride 10 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-9371-1)
(Preferred Pharmaceuticals, Inc.)
NDC Code
68788-9371-1
Package Description
10 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-9371-1)
Product NDC
68788-9371
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
Preferred Pharmaceuticals, Inc.
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/68788-9371-1