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TRAMADOL HYDROCHLORIDE

NDC 76420-245, TRAMADOL HYDROCHLORIDE, tablet, extended release, from Asclemed USA, Inc..

Product NDC
76420-245
Status
Listed
Labeler
Asclemed USA, Inc.
Dosage form
TABLET, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA201384
DEA schedule
CIV
Request
curl https://api.healthcare.dev/v1/drugs/ndc/76420-245 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • TRAMADOL HYDROCHLORIDE200 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
76420-245-307642002453030 TABLET, EXTENDED RELEASE in 1 BOTTLE (76420-245-30)
76420-245-607642002456060 TABLET, EXTENDED RELEASE in 1 BOTTLE (76420-245-60)
76420-245-907642002459090 TABLET, EXTENDED RELEASE in 1 BOTTLE (76420-245-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/dce0d21e-e4c2-4875-a2ce-9d53df190b80

Use it

Look up 76420-245 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/76420-245 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 76420-245. 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.