atomoxetine

Generic: atomoxetine

Labeler: a-s medication solutions
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name atomoxetine
Generic Name atomoxetine
Labeler a-s medication solutions
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

atomoxetine hydrochloride 40 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-6143
Product ID 50090-6143_a726ffd7-e7bd-4005-8b8a-b4d9bb58b67f
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA202682
Listing Expiration 2026-12-31
Marketing Start 2021-03-11

Pharmacologic Class

Classes
norepinephrine reuptake inhibitor [epc] norepinephrine uptake inhibitors [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 500906143
Hyphenated Format 50090-6143

Supplemental Identifiers

RxCUI
349594
UNII
57WVB6I2W0

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name atomoxetine (source: ndc)
Generic Name atomoxetine (source: ndc)
Application Number ANDA202682 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 40 mg/1
source: ndc
Packaging
  • 30 CAPSULE in 1 BOTTLE (50090-6143-0)
source: ndc

Packages (1)

50090-6143-0 30 CAPSULE in 1 BOTTLE (50090-6143-0)

Ingredients (1)

atomoxetine hydrochloride (40 mg/1)

Linked Drug Pages (1)

Atomoxetine ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "a726ffd7-e7bd-4005-8b8a-b4d9bb58b67f", "openfda": {"unii": ["57WVB6I2W0"], "rxcui": ["349594"], "spl_set_id": ["0782204e-56a3-4439-9fb8-194da9487049"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BOTTLE (50090-6143-0)", "package_ndc": "50090-6143-0", "marketing_start_date": "20221004"}], "brand_name": "Atomoxetine", "product_id": "50090-6143_a726ffd7-e7bd-4005-8b8a-b4d9bb58b67f", "dosage_form": "CAPSULE", "pharm_class": ["Norepinephrine Reuptake Inhibitor [EPC]", "Norepinephrine Uptake Inhibitors [MoA]"], "product_ndc": "50090-6143", "generic_name": "Atomoxetine", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Atomoxetine", "active_ingredients": [{"name": "ATOMOXETINE HYDROCHLORIDE", "strength": "40 mg/1"}], "application_number": "ANDA202682", "marketing_category": "ANDA", "marketing_start_date": "20210311", "listing_expiration_date": "20261231"}