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Nortriptyline Hydrochloride

NDC 70710-1153, Nortriptyline Hydrochloride, capsule, from Zydus Pharmaceuticals (USA) Inc..

Product NDC
70710-1153
Status
Listed
Labeler
Zydus Pharmaceuticals (USA) Inc.
Dosage form
CAPSULE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA213441
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70710-1153 \
  -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
70710-1153-170710115301100 CAPSULE in 1 BOTTLE (70710-1153-1)
70710-1153-37071011530330 CAPSULE in 1 BOTTLE (70710-1153-3)
70710-1153-570710115305500 CAPSULE in 1 BOTTLE (70710-1153-5)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/dbe85bdc-17a1-4201-bf48-a52e35d69b68

Use it

Look up 70710-1153 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70710-1153 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70710-1153. 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.