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"68788-7399-1" National Drug Code (NDC)
Duloxetine 10 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (68788-7399-1)
(Preferred Pharmaceuticals Inc.)
NDC Code
68788-7399-1
Package Description
10 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (68788-7399-1)
Product NDC
68788-7399
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
20160930
Marketing Category Name
ANDA
Application Number
ANDA203088
Manufacturer
Preferred Pharmaceuticals Inc.
Substance Name
DULOXETINE HYDROCHLORIDE
Strength
60
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/68788-7399-1