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PRAZIQUANTEL

NDC 49884-231, PRAZIQUANTEL, tablet, film coated, from Par Health USA, LLC.

Product NDC
49884-231
Status
Listed
Labeler
Par Health USA, LLC
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA208820
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/49884-231 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • PRAZIQUANTEL600 mg/1

Pharmacologic classes

Anthelmintic [EPC]

Package NDCNDC-11Package
49884-231-83498840231836 TABLET, FILM COATED in 1 BOTTLE (49884-231-83)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/16f2b9c4-a260-4a31-bd52-e5945913246c

  • NADAC price for package 49884023183

    GET /v1/drugs/nadac/49884023183

Use it

Look up 49884-231 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/49884-231 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 49884-231. 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.