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Tramadol Hydrochloride

NDC 59651-441, Tramadol Hydrochloride, tablet, film coated, from Aurobindo Pharma Limited.

Product NDC
59651-441
Status
Listed
Labeler
Aurobindo Pharma Limited
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA203494
DEA schedule
CIV
Request
curl https://api.healthcare.dev/v1/drugs/ndc/59651-441 \
  -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
59651-441-0159651044101100 TABLET, FILM COATED in 1 BOTTLE (59651-441-01)
59651-441-0559651044105500 TABLET, FILM COATED in 1 BOTTLE (59651-441-05)
59651-441-99596510441991000 TABLET, FILM COATED in 1 BOTTLE (59651-441-99)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/e5005d9e-91cb-4ff8-bcf2-b5ee70cf4f3f

Use it

Look up 59651-441 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/59651-441 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 59651-441. 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.