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TRAMADOL HYDROCHLORIDE

NDC 47335-531, TRAMADOL HYDROCHLORIDE, tablet, extended release, from Sun Pharmaceutical Industries, Inc..

Product NDC
47335-531
Status
Listed
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
TABLET, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA091607
DEA schedule
CIV
Request
curl https://api.healthcare.dev/v1/drugs/ndc/47335-531 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • TRAMADOL HYDROCHLORIDE100 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
47335-531-0847335053108100 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-531-08)
47335-531-18473350531181000 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-531-18)
47335-531-834733505318330 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-531-83)
47335-531-8847335053188100 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-531-88)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/dc420d50-6192-482d-b3da-3be55870a79a

Use it

Look up 47335-531 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/47335-531 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 47335-531. 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.