atomoxetine

Generic: atomoxetine

Labeler: bryant ranch prepack
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name atomoxetine
Generic Name atomoxetine
Labeler bryant ranch prepack
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

atomoxetine hydrochloride 25 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 72162-2543
Product ID 72162-2543_5992e5cd-c1d6-47a1-9a9a-ed2ff4d6f207
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA079021
Listing Expiration 2026-12-31
Marketing Start 2025-07-01

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 721622543
Hyphenated Format 72162-2543

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 ANDA079021 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 25 mg/1
source: ndc
Packaging
  • 30 CAPSULE in 1 BOTTLE (72162-2543-3)
source: ndc

Packages (1)

72162-2543-3 30 CAPSULE in 1 BOTTLE (72162-2543-3)

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": "5992e5cd-c1d6-47a1-9a9a-ed2ff4d6f207", "openfda": {"unii": ["57WVB6I2W0"], "rxcui": ["349593"], "spl_set_id": ["bb2c12e4-563c-417e-bee1-6d8c51e75af4"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BOTTLE (72162-2543-3)", "package_ndc": "72162-2543-3", "marketing_start_date": "20251016"}], "brand_name": "Atomoxetine", "product_id": "72162-2543_5992e5cd-c1d6-47a1-9a9a-ed2ff4d6f207", "dosage_form": "CAPSULE", "pharm_class": ["Norepinephrine Reuptake Inhibitor [EPC]", "Norepinephrine Uptake Inhibitors [MoA]"], "product_ndc": "72162-2543", "generic_name": "Atomoxetine", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Atomoxetine", "active_ingredients": [{"name": "ATOMOXETINE HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "ANDA079021", "marketing_category": "ANDA", "marketing_start_date": "20250701", "listing_expiration_date": "20261231"}