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Atomoxetine Hydrochloride

NDC 60505-2835, atomoxetine hydrochloride, capsule, from Apotex Corp..

Product NDC
60505-2835
Status
Listed
Labeler
Apotex Corp.
Dosage form
CAPSULE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA078983
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/60505-2835 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • ATOMOXETINE HYDROCHLORIDE80 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
60505-2835-36050528350330 CAPSULE in 1 BOTTLE (60505-2835-3)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/132852a6-5bff-15dd-255c-98309dd83630

  • NADAC price for package 60505283503

    GET /v1/drugs/nadac/60505283503

Use it

Look up 60505-2835 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/60505-2835 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 60505-2835. 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.