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"68788-8362-3" National Drug Code (NDC)

Duloxetine 30 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (68788-8362-3)
(Preferred Pharmaceuticals Inc.)

NDC Code68788-8362-3
Package Description30 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (68788-8362-3)
Product NDC68788-8362
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameDuloxetine
Proprietary Name SuffixDelayed-release
Non-Proprietary NameDuloxetine Hydrochloride
Dosage FormCAPSULE, DELAYED RELEASE PELLETS
UsageORAL
Start Marketing Date20230201
Marketing Category NameANDA
Application NumberANDA203088
ManufacturerPreferred Pharmaceuticals Inc.
Substance NameDULOXETINE HYDROCHLORIDE
Strength40
Strength Unitmg/1
Pharmacy ClassesNorepinephrine 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/68788-8362-3





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