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Phenazopyridine Hydrochloride

NDC 70518-3975, Phenazopyridine Hydrochloride, tablet, from REMEDYREPACK INC..

Product NDC
70518-3975
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/70518-3975 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • PHENAZOPYRIDINE HYDROCHLORIDE200 mg/1
Package NDCNDC-11Package
70518-3975-07051839750030 TABLET in 1 BLISTER PACK (70518-3975-0)
70518-3975-2705183975029 TABLET in 1 BOTTLE, PLASTIC (70518-3975-2)
70518-3975-3705183975036 TABLET in 1 BOTTLE, PLASTIC (70518-3975-3)
70518-3975-47051839750450 POUCH in 1 BOX (70518-3975-4) / 1 TABLET in 1 POUCH (70518-3975-5)
70518-3975-670518397506100 POUCH in 1 BOX (70518-3975-6) / 1 TABLET in 1 POUCH (70518-3975-5)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/6eb59b69-4ad0-47b1-bd3c-1d04d0852ec5

Use it

Look up 70518-3975 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70518-3975 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70518-3975. 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.