NDC 71335-2017

Duloxetine

Duloxetine

Duloxetine is a Oral Capsule, Delayed Release in the Human Prescription Drug category. It is labeled and distributed by Bryant Ranch Prepack. The primary component is Duloxetine Hydrochloride.

Product ID71335-2017_4cada99d-73c4-4499-8b43-4d872f28dcfe
NDC71335-2017
Product TypeHuman Prescription Drug
Proprietary NameDuloxetine
Generic NameDuloxetine
Dosage FormCapsule, Delayed Release
Route of AdministrationORAL
Marketing Start Date2017-03-16
Marketing CategoryANDA /
Application NumberANDA208706
Labeler NameBryant Ranch Prepack
Substance NameDULOXETINE HYDROCHLORIDE
Active Ingredient Strength30 mg/1
Pharm ClassesNorepinephrine Uptake Inhibitors [MoA], Serotonin Uptake Inhibitors [MoA], Serotonin and Norepinephrine Reuptake Inhibitor [EPC]
NDC Exclude FlagN
Listing Certified Through2023-12-31

Packaging

NDC 71335-2017-1

30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-2017-1)
Marketing Start Date2022-02-10
NDC Exclude FlagN
Sample Package?N

Drug Details

NDC Crossover Matching brand name "Duloxetine" or generic name "Duloxetine"

NDCBrand NameGeneric Name
0093-7542DuloxetineDuloxetine
0093-7543DuloxetineDuloxetine
0093-7544DuloxetineDuloxetine
0228-2890DuloxetineDuloxetine
0228-2891DuloxetineDuloxetine
0228-2892DuloxetineDuloxetine
0904-7043DuloxetineDuloxetine Hydrochloride
0904-7044DuloxetineDuloxetine Hydrochloride
0904-7045DuloxetineDuloxetine Hydrochloride
23155-654duloxetineduloxetine
23155-655duloxetineduloxetine
23155-656duloxetineduloxetine
25000-608DuloxetineDuloxetine Hydrochloride
25000-609DuloxetineDuloxetine Hydrochloride
25000-610DuloxetineDuloxetine Hydrochloride
27241-097DuloxetineDuloxetine
27241-098DuloxetineDuloxetine
67877-264DuloxetineDuloxetine
67877-265DuloxetineDuloxetine
67877-263DuloxetineDuloxetine
68001-255DuloxetineDuloxetine
68001-256DuloxetineDuloxetine
68001-257DuloxetineDuloxetine
68071-4700DuloxetineDuloxetine
68084-692DuloxetineDuloxetine
68084-675DuloxetineDuloxetine
68084-683DuloxetineDuloxetine
68151-4727DuloxetineDuloxetine
68180-294DuloxetineDuloxetine
68180-297DuloxetineDuloxetine
68180-295DuloxetineDuloxetine
68180-296DuloxetineDuloxetine
68382-385DuloxetineDuloxetine
68382-386DuloxetineDuloxetine
68382-387DuloxetineDuloxetine
68788-6427duloxetineduloxetine
68788-9262DuloxetineDuloxetine
68788-9266DuloxetineDuloxetine
69097-298duloxetineduloxetine
69097-297duloxetineduloxetine
69097-299duloxetineduloxetine
70518-0491DuloxetineDuloxetine
70518-1066DuloxetineDuloxetine
70518-0937DuloxetineDuloxetine
70518-1054DuloxetineDuloxetine
70518-1139DuloxetineDuloxetine
70518-0685DuloxetineDuloxetine
70518-1128DULOXETINEDULOXETINE
70518-1011DuloxetineDuloxetine
70518-1244DuloxetineDuloxetine

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