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Atomoxetine

NDC 65862-239, Atomoxetine, capsule, from Aurobindo Pharma Limited.

Product NDC
65862-239
Status
Listed
Labeler
Aurobindo Pharma Limited
Dosage form
CAPSULE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA079016
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/65862-239 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • ATOMOXETINE HYDROCHLORIDE18 mg/1

Pharmacologic classes

Norepinephrine Reuptake Inhibitor [EPC]; Norepinephrine Uptake Inhibitors [MoA]

Package NDCNDC-11Package
65862-239-22658620239222000 CAPSULE in 1 BOTTLE (65862-239-22)
65862-239-306586202393030 CAPSULE in 1 BOTTLE (65862-239-30)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/6f6bea0c-297b-43ff-8960-ecc11243e06e

Use it

Look up 65862-239 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/65862-239 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 65862-239. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
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Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.