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Atomoxetine

NDC 71335-2162, Atomoxetine, capsule, from Bryant Ranch Prepack.

Product NDC
71335-2162
Status
Listed
Labeler
Bryant Ranch Prepack
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/71335-2162 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • ATOMOXETINE HYDROCHLORIDE40 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
71335-2162-17133521620130 CAPSULE in 1 BOTTLE (71335-2162-1)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/d4fe9217-1853-4f8b-9a93-77e511554ca1

Use it

Look up 71335-2162 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71335-2162 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71335-2162. 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.