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Tramadol Hydrochloride

NDC 52817-195, Tramadol Hydrochloride, tablet, coated, from TRUPHARMA LLC.

Product NDC
52817-195
Status
Listed
Labeler
TRUPHARMA LLC
Dosage form
TABLET, COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA208708
DEA schedule
CIV
Request
curl https://api.healthcare.dev/v1/drugs/ndc/52817-195 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • TRAMADOL HYDROCHLORIDE50 mg/1

Pharmacologic classes

Full Opioid Agonists [MoA]; Opioid Agonist [EPC]

Package NDCNDC-11Package
52817-195-00528170195001000 TABLET, COATED in 1 BOTTLE (52817-195-00)
52817-195-1052817019510100 TABLET, COATED in 1 BOTTLE (52817-195-10)
52817-195-5052817019550500 TABLET, COATED in 1 BOTTLE (52817-195-50)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/61fb5ba7-6896-4ee4-83de-caee69b06a8e

Use it

Look up 52817-195 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/52817-195 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 52817-195. 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.