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atomoxetine

NDC 68462-265, atomoxetine, capsule, from Glenmark Pharmaceuticals Inc., USA.

Product NDC
68462-265
Status
Listed
Labeler
Glenmark Pharmaceuticals Inc., USA
Dosage form
CAPSULE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA079019
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/68462-265 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • ATOMOXETINE HYDROCHLORIDE10 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
68462-265-23684620265232000 CAPSULE in 1 BOTTLE (68462-265-23)
68462-265-306846202653030 CAPSULE in 1 BOTTLE (68462-265-30)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/0ab8d905-e890-4e91-a730-3e5d12f5c23f

  • NADAC price for package 68462026530

    GET /v1/drugs/nadac/68462026530

Use it

Look up 68462-265 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68462-265 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68462-265. 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.