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Amitriptyline Hydrochloride

NDC 76420-697, Amitriptyline Hydrochloride, tablet, film coated, from Asclemed USA, Inc..

Product NDC
76420-697
Status
Listed
Labeler
Asclemed USA, Inc.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA214548
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/76420-697 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • AMITRIPTYLINE HYDROCHLORIDE100 mg/1

Pharmacologic classes

Tricyclic Antidepressant [EPC]

Package NDCNDC-11Package
76420-697-0176420069701100 TABLET, FILM COATED in 1 BOTTLE (76420-697-01)
76420-697-307642006973030 TABLET, FILM COATED in 1 BOTTLE (76420-697-30)
76420-697-607642006976060 TABLET, FILM COATED in 1 BOTTLE (76420-697-60)
76420-697-907642006979090 TABLET, FILM COATED in 1 BOTTLE (76420-697-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/776d2c2c-d897-4da1-a99a-b4324e1f864f

Use it

Look up 76420-697 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/76420-697 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 76420-697. 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.