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Meperidine Hydrochloride

NDC 64950-214, Meperidine Hydrochloride, tablet, from Genus Lifesciences Inc..

Product NDC
64950-214
Status
Listed
Labeler
Genus Lifesciences Inc.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA040893
DEA schedule
CII
Request
curl https://api.healthcare.dev/v1/drugs/ndc/64950-214 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • MEPERIDINE HYDROCHLORIDE50 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
64950-214-0164950021401100 TABLET in 1 BOTTLE, PLASTIC (64950-214-01)
64950-214-036495002140330 TABLET in 1 BOTTLE, PLASTIC (64950-214-03)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/792fefda-6cc4-4709-b902-fd9787fc310a

Use it

Look up 64950-214 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/64950-214 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 64950-214. 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.