www.ndcvalidator.com
National Drug Code Lookup | NDC Directory | About | Feedback

"47335-382-61" National Drug Code (NDC)

Duloxetine 100 BLISTER PACK in 1 CARTON (47335-382-61) > 1 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK
(Sun Pharmaceutical Industries, Inc.)

NDC Code47335-382-61
Package Description100 BLISTER PACK in 1 CARTON (47335-382-61) > 1 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK
Product NDC47335-382
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameDuloxetine
Non-Proprietary NameDuloxetine
Dosage FormCAPSULE, DELAYED RELEASE
UsageORAL
Start Marketing Date20131211
Marketing Category NameANDA
Application NumberANDA090745
ManufacturerSun Pharmaceutical Industries, Inc.
Substance NameDULOXETINE HYDROCHLORIDE
Strength30
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/47335-382-61





Copyright © 2007-2024 www.ndcvalidator.com