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Methenamine Hippurate

NDC 42571-332, Methenamine Hippurate, tablet, from Micro Labs Limited.

Product NDC
42571-332
Status
Listed
Labeler
Micro Labs Limited
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA212172
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/42571-332 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • METHENAMINE HIPPURATE1000 mg/1
Package NDCNDC-11Package
42571-332-0142571033201100 TABLET in 1 BOTTLE (42571-332-01)
42571-332-234257103322380 TABLET in 1 CARTON (42571-332-23)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/e07ddd63-4725-49db-bec2-bd4f966c6e48

  • NADAC price for package 42571033201

    GET /v1/drugs/nadac/42571033201

Use it

Look up 42571-332 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/42571-332 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 42571-332. 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.