NDC 80425-0012

Duloxetine HCL DR

Duloxetine Hcl

Duloxetine HCL DR is a Oral Capsule, Delayed Release in the Human Prescription Drug category. It is labeled and distributed by Advanced Rx Pharmacy Of Tennessee, Llc. The primary component is Duloxetine Hydrochloride.

Product ID80425-0012_b0247207-6668-40dc-e053-2a95a90a676f
NDC80425-0012
Product TypeHuman Prescription Drug
Proprietary NameDuloxetine HCL DR
Generic NameDuloxetine Hcl
Dosage FormCapsule, Delayed Release
Route of AdministrationORAL
Marketing Start Date2012-05-01
Marketing CategoryANDA /
Application NumberANDA203197
Labeler NameAdvanced Rx Pharmacy of Tennessee, LLC
Substance NameDULOXETINE HYDROCHLORIDE
Active Ingredient Strength30 mg/1
Pharm ClassesNorepinephrine Uptake Inhibitors [MoA],Serotonin and Norepinephrine Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]
NDC Exclude FlagN
Listing Certified Through2022-12-31

Packaging

NDC 80425-0012-1

30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (80425-0012-1)
Marketing Start Date2020-09-25
NDC Exclude FlagN
Sample Package?N

Drug Details

NDC Crossover Matching brand name "Duloxetine HCL DR" or generic name "Duloxetine Hcl"

NDCBrand NameGeneric Name
80425-0086CymbaltaDuloxetine HCl
80425-0012Duloxetine HCLDuloxetine HCL
80425-0013Duloxetine HCLDuloxetine HCL
80425-0014Duloxetine HCLDuloxetine HCL
80425-0146Duloxetine HCLDuloxetine HCL

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.