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atomoxetine

NDC 68382-218, atomoxetine, capsule, from Zydus Pharmaceuticals USA Inc..

Product NDC
68382-218
Status
Listed
Labeler
Zydus Pharmaceuticals USA Inc.
Dosage form
CAPSULE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA079017
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/68382-218 \
  -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
68382-218-02683820218022000 CAPSULE in 1 BOTTLE (68382-218-02)
68382-218-066838202180630 CAPSULE in 1 BOTTLE (68382-218-06)
68382-218-10683820218101000 CAPSULE in 1 BOTTLE (68382-218-10)
68382-218-146838202181460 CAPSULE in 1 BOTTLE (68382-218-14)
68382-218-166838202181690 CAPSULE in 1 BOTTLE (68382-218-16)
68382-218-776838202187710 BLISTER PACK in 1 CARTON (68382-218-77) / 10 CAPSULE in 1 BLISTER PACK (68382-218-30)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/5f89c7c9-4c25-4ba2-ad90-5aeadb48f214

Use it

Look up 68382-218 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68382-218 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68382-218. 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.