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Metronidazole

NDC 70518-3265, METRONIDAZOLE, tablet, from REMEDYREPACK INC..

Product NDC
70518-3265
Status
Listed
Labeler
REMEDYREPACK INC.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA205245
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70518-3265 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • METRONIDAZOLE500 mg/1

Pharmacologic classes

Nitroimidazole Antimicrobial [EPC]; Nitroimidazoles [CS]

Package NDCNDC-11Package
70518-3265-1705183265014 TABLET in 1 BOTTLE, PLASTIC (70518-3265-1)
70518-3265-27051832650214 TABLET in 1 BOTTLE, PLASTIC (70518-3265-2)
70518-3265-47051832650420 TABLET in 1 BOTTLE, PLASTIC (70518-3265-4)
70518-3265-57051832650530 TABLET in 1 BLISTER PACK (70518-3265-5)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/5cc3fd98-d579-432e-a4b5-b6d5586991a6

Use it

Look up 70518-3265 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70518-3265 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70518-3265. 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.