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Moxifloxacin Hydrochloride Tablets, 400 mg

NDC 70518-4312, Moxifloxacin Hydrochloride Tablets, 400 mg, tablet, film coated, from REMEDYREPACK INC..

Product NDC
70518-4312
Status
Listed
Labeler
REMEDYREPACK INC.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA208682
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70518-4312 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • MOXIFLOXACIN HYDROCHLORIDE MONOHYDRATE400 mg/1

Pharmacologic classes

Fluoroquinolone Antibacterial [EPC]; Fluoroquinolones [CS]

Package NDCNDC-11Package
70518-4312-0705184312007 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4312-0)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/bdb3f89a-01e7-411d-b071-48e87def0873

Use it

Look up 70518-4312 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70518-4312 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70518-4312. 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.