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TRAMADOL HYDROCHLORIDE

NDC 76420-536, TRAMADOL HYDROCHLORIDE, tablet, extended release, from Asclemed USA, Inc..

Product NDC
76420-536
Status
Listed
Labeler
Asclemed USA, Inc.
Dosage form
TABLET, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA200503
DEA schedule
CIV
Request
curl https://api.healthcare.dev/v1/drugs/ndc/76420-536 \
  -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
76420-536-307642005363030 TABLET, EXTENDED RELEASE in 1 BOTTLE (76420-536-30)
76420-536-607642005366060 TABLET, EXTENDED RELEASE in 1 BOTTLE (76420-536-60)
76420-536-907642005369090 TABLET, EXTENDED RELEASE in 1 BOTTLE (76420-536-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/a26ca887-e26c-4c32-8dbd-1fa2eb6db9dc

Use it

Look up 76420-536 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/76420-536 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 76420-536. 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.