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Phenazopyridine Hydrochloride

NDC 70518-3868, Phenazopyridine, tablet, from REMEDYREPACK INC..

Product NDC
70518-3868
Status
Listed
Labeler
REMEDYREPACK INC.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
UNAPPROVED DRUG OTHER
Application
—
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70518-3868 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • PHENAZOPYRIDINE HYDROCHLORIDE200 mg/1
Package NDCNDC-11Package
70518-3868-17051838680121 TABLET in 1 BOTTLE, PLASTIC (70518-3868-1)
70518-3868-37051838680330 TABLET in 1 BLISTER PACK (70518-3868-3)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/82dc87bb-ba27-4b86-9bc9-18492975ac9f

Use it

Look up 70518-3868 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70518-3868 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70518-3868. 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.