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TRAMADOL HYDROCHLORIDE

NDC 71205-656, TRAMADOL HYDROCHLORIDE, tablet, extended release, from Proficient Rx LP.

Product NDC
71205-656
Status
Listed
Labeler
Proficient Rx LP
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/71205-656 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • TRAMADOL HYDROCHLORIDE300 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
71205-656-307120506563030 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-656-30)
71205-656-607120506566060 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-656-60)
71205-656-907120506569090 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-656-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/68646295-49b2-45ac-bf19-99bb91f7333d

Use it

Look up 71205-656 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71205-656 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71205-656. 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.