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 25 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-7342
Product ID 50090-7342_c6e62eb1-c864-4e73-8908-0d3646ba58cf
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA079019
Listing Expiration 2026-12-31
Marketing Start 2017-05-30

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 500907342
Hyphenated Format 50090-7342

Supplemental Identifiers

RxCUI
349593
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 ANDA079019 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 25 mg/1
source: ndc
Packaging
  • 30 CAPSULE in 1 BOTTLE (50090-7342-0)
source: ndc

Packages (1)

50090-7342-0 30 CAPSULE in 1 BOTTLE (50090-7342-0)

Ingredients (1)

atomoxetine hydrochloride (25 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": "c6e62eb1-c864-4e73-8908-0d3646ba58cf", "openfda": {"unii": ["57WVB6I2W0"], "rxcui": ["349593"], "spl_set_id": ["47f6faeb-52b5-4b04-bf34-de5db8eb46dc"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BOTTLE (50090-7342-0)", "package_ndc": "50090-7342-0", "marketing_start_date": "20241016"}], "brand_name": "atomoxetine", "product_id": "50090-7342_c6e62eb1-c864-4e73-8908-0d3646ba58cf", "dosage_form": "CAPSULE", "pharm_class": ["Norepinephrine Reuptake Inhibitor [EPC]", "Norepinephrine Uptake Inhibitors [MoA]"], "product_ndc": "50090-7342", "generic_name": "atomoxetine", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "atomoxetine", "active_ingredients": [{"name": "ATOMOXETINE HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "ANDA079019", "marketing_category": "ANDA", "marketing_start_date": "20170530", "listing_expiration_date": "20261231"}