atomoxetine
Generic: atomoxetine
Labeler: bryant ranch prepackDrug Facts
Product Profile
Brand Name
atomoxetine
Generic Name
atomoxetine
Labeler
bryant ranch prepack
Dosage Form
CAPSULE
Routes
Active Ingredients
atomoxetine hydrochloride 60 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
71335-9702
Product ID
71335-9702_377c2023-4cbd-cc01-e063-6294a90a7c68
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA079016
Listing Expiration
2026-12-31
Marketing Start
2017-05-30
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
713359702
Hyphenated Format
71335-9702
Supplemental Identifiers
RxCUI
UNII
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
source: ndc
Resolved Composition
Strengths
- 60 mg/1
Packaging
- 30 CAPSULE in 1 BOTTLE (71335-9702-1)
- 60 CAPSULE in 1 BOTTLE (71335-9702-2)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "377c2023-4cbd-cc01-e063-6294a90a7c68", "openfda": {"unii": ["57WVB6I2W0"], "rxcui": ["349595"], "spl_set_id": ["35b42f0c-a183-478b-bced-652dc12b33ec"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BOTTLE (71335-9702-1)", "package_ndc": "71335-9702-1", "marketing_start_date": "20230428"}, {"sample": false, "description": "60 CAPSULE in 1 BOTTLE (71335-9702-2)", "package_ndc": "71335-9702-2", "marketing_start_date": "20250612"}], "brand_name": "Atomoxetine", "product_id": "71335-9702_377c2023-4cbd-cc01-e063-6294a90a7c68", "dosage_form": "CAPSULE", "pharm_class": ["Norepinephrine Reuptake Inhibitor [EPC]", "Norepinephrine Uptake Inhibitors [MoA]"], "product_ndc": "71335-9702", "generic_name": "Atomoxetine", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Atomoxetine", "active_ingredients": [{"name": "ATOMOXETINE HYDROCHLORIDE", "strength": "60 mg/1"}], "application_number": "ANDA079016", "marketing_category": "ANDA", "marketing_start_date": "20170530", "listing_expiration_date": "20261231"}