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"31722-170-31" National Drug Code (NDC)

Duloxetine 7 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK (31722-170-31)
(Camber Pharmaceuticals, Inc.)

NDC Code31722-170-31
Package Description7 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK (31722-170-31)
Product NDC31722-170
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameDuloxetine
Non-Proprietary NameDuloxetine
Dosage FormCAPSULE, DELAYED RELEASE
UsageORAL
Start Marketing Date20201230
Marketing Category NameANDA
Application NumberANDA204343
ManufacturerCamber Pharmaceuticals, Inc.
Substance NameDULOXETINE HYDROCHLORIDE
Strength60
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/31722-170-31





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