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Nitrofurantoin

NDC 59651-206, Nitrofurantoin, suspension, from Aurobindo Pharma Limited.

Product NDC
59651-206
Status
Listed
Labeler
Aurobindo Pharma Limited
Dosage form
SUSPENSION
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA212607
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/59651-206 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • NITROFURANTOIN MONOHYDRATE25 mg/5mL

Pharmacologic classes

Nitrofuran Antibacterial [EPC]; Nitrofurans [CS]

Package NDCNDC-11Package
59651-206-23596510206231 BOTTLE in 1 CARTON (59651-206-23) / 230 mL in 1 BOTTLE

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/e9d10eaa-cf9c-469e-82ef-5af7285f2c86

  • NADAC price for package 59651020623

    GET /v1/drugs/nadac/59651020623

Use it

Look up 59651-206 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/59651-206 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 59651-206. 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.