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NDC 50090-4236-00 Atomoxetine Hydrochloride 40 mg/1 Details

Atomoxetine Hydrochloride 40 mg/1

Atomoxetine Hydrochloride is a ORAL CAPSULE in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by A-S Medication Solutions. The primary component is ATOMOXETINE HYDROCHLORIDE.

MedlinePlus Drug Summary

Atomoxetine is used as part of a total treatment program to increase the ability to pay attention and decrease impulsiveness and hyperactivity in children and adults with ADHD. Atomoxetine is in a class of medications called selective norepinephrine reuptake inhibitors. It works by increasing the levels of norepinephrine, a natural substance in the brain that is needed to control behavior.

Related Packages: 50090-4236-00
Last Updated: 11/30/2022
MedLinePlus Full Drug Details: Atomoxetine

Product Information

NDC	50090-4236
Product ID	50090-4236_d1a130e7-3cee-40cf-a4c6-cb3893304987
Associated GPIs
GCN Sequence Number	n/a
GCN Sequence Number Description	n/a
HIC3	n/a
HIC3 Description	n/a
GCN	n/a
HICL Sequence Number	n/a
HICL Sequence Number Description	n/a
Brand/Generic	n/a
Proprietary Name	Atomoxetine Hydrochloride
Proprietary Name Suffix	n/a
Non-Proprietary Name	atomoxetine hydrochloride
Product Type	HUMAN PRESCRIPTION DRUG
Dosage Form	CAPSULE
Route	ORAL
Active Ingredient Strength	40
Active Ingredient Units	mg/1
Substance Name	ATOMOXETINE HYDROCHLORIDE
Labeler Name	A-S Medication Solutions
Pharmaceutical Class	Norepinephrine Reuptake Inhibitor [EPC], Norepinephrine Uptake Inhibitors [MoA]
DEA Schedule	n/a
Marketing Category	ANDA
Application Number	ANDA078983
Listing Certified Through	2024-12-31

Package

NDC 50090-4236-00 (50090423600)

Pricing Information	N/A
NDC Package Code	50090-4236-0
Billing NDC	50090423600
Package	30 CAPSULE in 1 BOTTLE (50090-4236-0)
Marketing Start Date	2019-03-29
NDC Exclude Flag	N