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Protriptyline Hydrochloride

NDC 42806-097, Protriptyline Hydrochloride, tablet, film coated, from Epic Pharma, LLC.

Product NDC
42806-097
Status
Listed
Labeler
Epic Pharma, LLC
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA202220
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/42806-097 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • PROTRIPTYLINE HYDROCHLORIDE10 mg/1

Pharmacologic classes

Tricyclic Antidepressant [EPC]

Package NDCNDC-11Package
42806-097-0142806009701100 TABLET, FILM COATED in 1 BOTTLE (42806-097-01)
42806-097-10428060097101000 TABLET, FILM COATED in 1 BOTTLE (42806-097-10)
42806-097-304280600973030 TABLET, FILM COATED in 1 BOTTLE (42806-097-30)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/c6c7c39e-e510-4f4a-bf7a-926f0e075d3a

  • NADAC price for package 42806009730

    GET /v1/drugs/nadac/42806009730

Use it

Look up 42806-097 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/42806-097 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 42806-097. 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.