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Nitrofurantoin

NDC 70069-829, Nitrofurantoin, for suspension, from Somerset Therapeutics, LLC.

Product NDC
70069-829
Status
Listed
Labeler
Somerset Therapeutics, LLC
Dosage form
FOR SUSPENSION
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA208909
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70069-829 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • NITROFURANTOIN25 mg/5mL

Pharmacologic classes

Nitrofuran Antibacterial [EPC]; Nitrofurans [CS]

Package NDCNDC-11Package
70069-829-01700690829011 BOTTLE, GLASS in 1 CARTON (70069-829-01) / 230 mL in 1 BOTTLE, GLASS

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/dd99ba40-edff-47c3-9ee4-7e5b7774e5b5

  • NADAC price for package 70069082901

    GET /v1/drugs/nadac/70069082901

Use it

Look up 70069-829 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70069-829 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70069-829. 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.