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 100 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-6144
Product ID 50090-6144_3378441e-e572-45a8-89d5-861d2e6cb11d
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 500906144
Hyphenated Format 50090-6144

Supplemental Identifiers

RxCUI
608139
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
  • 100 mg/1
source: ndc
Packaging
  • 30 CAPSULE in 1 BOTTLE (50090-6144-0)
source: ndc

Packages (1)

50090-6144-0 30 CAPSULE in 1 BOTTLE (50090-6144-0)

Ingredients (1)

atomoxetine hydrochloride (100 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": "3378441e-e572-45a8-89d5-861d2e6cb11d", "openfda": {"unii": ["57WVB6I2W0"], "rxcui": ["608139"], "spl_set_id": ["14fb8a4c-c2bf-4d44-bea9-cd159c2ca5fa"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BOTTLE (50090-6144-0)", "package_ndc": "50090-6144-0", "marketing_start_date": "20221004"}], "brand_name": "Atomoxetine", "product_id": "50090-6144_3378441e-e572-45a8-89d5-861d2e6cb11d", "dosage_form": "CAPSULE", "pharm_class": ["Norepinephrine Reuptake Inhibitor [EPC]", "Norepinephrine Uptake Inhibitors [MoA]"], "product_ndc": "50090-6144", "generic_name": "Atomoxetine", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Atomoxetine", "active_ingredients": [{"name": "ATOMOXETINE HYDROCHLORIDE", "strength": "100 mg/1"}], "application_number": "ANDA202682", "marketing_category": "ANDA", "marketing_start_date": "20210311", "listing_expiration_date": "20261231"}