atomoxetine
Generic: atomoxetine
Labeler: american health packagingDrug Facts
Product Profile
Brand Name
atomoxetine
Generic Name
atomoxetine
Labeler
american health packaging
Dosage Form
CAPSULE
Routes
Active Ingredients
atomoxetine hydrochloride 40 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
60687-326
Product ID
60687-326_2759be5a-a8a1-2119-e063-6394a90a38ac
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA079016
Listing Expiration
2026-12-31
Marketing Start
2017-09-08
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
60687326
Hyphenated Format
60687-326
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
- 40 mg/1
Packaging
- 30 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-326-25) / 1 CAPSULE in 1 BLISTER PACK (60687-326-95)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2759be5a-a8a1-2119-e063-6394a90a38ac", "openfda": {"unii": ["57WVB6I2W0"], "rxcui": ["349593", "349594"], "spl_set_id": ["10d36b32-0202-4c03-8a1a-cd5d53f231e7"], "manufacturer_name": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "30 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-326-25) / 1 CAPSULE in 1 BLISTER PACK (60687-326-95)", "package_ndc": "60687-326-25", "marketing_start_date": "20170908"}], "brand_name": "Atomoxetine", "product_id": "60687-326_2759be5a-a8a1-2119-e063-6394a90a38ac", "dosage_form": "CAPSULE", "pharm_class": ["Norepinephrine Reuptake Inhibitor [EPC]", "Norepinephrine Uptake Inhibitors [MoA]"], "product_ndc": "60687-326", "generic_name": "Atomoxetine", "labeler_name": "American Health Packaging", "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": "20170908", "listing_expiration_date": "20261231"}