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Nortriptyline Hydrochloride

NDC 51672-4001, Nortriptyline Hydrochloride, capsule, from Sun Pharmaceutical Industries, Inc..

Product NDC
51672-4001
Status
Listed
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
CAPSULE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA075520
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/51672-4001 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • NORTRIPTYLINE HYDROCHLORIDE10 mg/1

Pharmacologic classes

Tricyclic Antidepressant [EPC]

Package NDCNDC-11Package
51672-4001-151672400101100 CAPSULE in 1 BOTTLE (51672-4001-1)
51672-4001-251672400102500 CAPSULE in 1 BOTTLE (51672-4001-2)
51672-4001-55167240010590 CAPSULE in 1 BOTTLE (51672-4001-5)
51672-4001-65167240010630 CAPSULE in 1 BOTTLE (51672-4001-6)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/aee2c1a1-d848-4c3b-8c6d-8a4f6ce94c28

Use it

Look up 51672-4001 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/51672-4001 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 51672-4001. 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.