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 40 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 71335-2162
Product ID 71335-2162_3767a887-2273-a522-e063-6394a90a3fbc
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA079016
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 713352162
Hyphenated Format 71335-2162

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 ANDA079016 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 40 mg/1
source: ndc
Packaging
  • 30 CAPSULE in 1 BOTTLE (71335-2162-1)
source: ndc

Packages (1)

71335-2162-1 30 CAPSULE in 1 BOTTLE (71335-2162-1)

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": "3767a887-2273-a522-e063-6394a90a3fbc", "openfda": {"unii": ["57WVB6I2W0"], "rxcui": ["349594"], "spl_set_id": ["d4fe9217-1853-4f8b-9a93-77e511554ca1"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BOTTLE (71335-2162-1)", "package_ndc": "71335-2162-1", "marketing_start_date": "20220907"}], "brand_name": "Atomoxetine", "product_id": "71335-2162_3767a887-2273-a522-e063-6394a90a3fbc", "dosage_form": "CAPSULE", "pharm_class": ["Norepinephrine Reuptake Inhibitor [EPC]", "Norepinephrine Uptake Inhibitors [MoA]"], "product_ndc": "71335-2162", "generic_name": "Atomoxetine", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Atomoxetine", "active_ingredients": [{"name": "ATOMOXETINE HYDROCHLORIDE", "strength": "40 mg/1"}], "application_number": "ANDA079016", "marketing_category": "ANDA", "marketing_start_date": "20170530", "listing_expiration_date": "20261231"}