atomoxetine

Generic: atomoxetine

Labeler: american health packaging
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name atomoxetine
Generic Name atomoxetine
Labeler american health packaging
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

atomoxetine hydrochloride 25 mg/1

Manufacturer
American Health Packaging

Identifiers & Regulatory

Product NDC 60687-567
Product ID 60687-567_2759be5a-a8a1-2119-e063-6394a90a38ac
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA079016
Listing Expiration 2026-12-31
Marketing Start 2020-12-07

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 60687567
Hyphenated Format 60687-567

Supplemental Identifiers

RxCUI
349593 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
  • 25 mg/1
source: ndc
Packaging
  • 30 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-567-21) / 1 CAPSULE in 1 BLISTER PACK (60687-567-11)
source: ndc

Packages (1)

Ingredients (1)

atomoxetine hydrochloride (25 mg/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 (60687-567-21)  / 1 CAPSULE in 1 BLISTER PACK (60687-567-11)", "package_ndc": "60687-567-21", "marketing_start_date": "20201207"}], "brand_name": "Atomoxetine", "product_id": "60687-567_2759be5a-a8a1-2119-e063-6394a90a38ac", "dosage_form": "CAPSULE", "pharm_class": ["Norepinephrine Reuptake Inhibitor [EPC]", "Norepinephrine Uptake Inhibitors [MoA]"], "product_ndc": "60687-567", "generic_name": "Atomoxetine", "labeler_name": "American Health Packaging", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Atomoxetine", "active_ingredients": [{"name": "ATOMOXETINE HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "ANDA079016", "marketing_category": "ANDA", "marketing_start_date": "20201207", "listing_expiration_date": "20261231"}