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Amitriptyline Hydrochloride

NDC 57664-690, Amitriptyline Hydrochloride, tablet, film coated, from Sun Pharmaceutical Industries, Inc..

Product NDC
57664-690
Status
Listed
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA089399
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/57664-690 \
  -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
57664-690-8857664069088100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (57664-690-88)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/4e520c63-1cf6-40f6-a51c-3f9b0e181342

  • NADAC price for package 57664069088

    GET /v1/drugs/nadac/57664069088

Use it

Look up 57664-690 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/57664-690 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 57664-690. 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.