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Moxifloxacin

NDC 31722-845, Moxifloxacin, tablet, film coated, from Camber Pharmaceuticals, Inc..

Product NDC
31722-845
Status
Listed
Labeler
Camber Pharmaceuticals, Inc.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA204836
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/31722-845 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • MOXIFLOXACIN HYDROCHLORIDE400 mg/1

Pharmacologic classes

Fluoroquinolone Antibacterial [EPC]; Fluoroquinolones [CS]

Package NDCNDC-11Package
31722-845-0531722084505500 TABLET, FILM COATED in 1 BOTTLE (31722-845-05)
31722-845-303172208453030 TABLET, FILM COATED in 1 BOTTLE (31722-845-30)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/1e6bc886-eec9-4cd8-be78-7563817457f2

Use it

Look up 31722-845 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/31722-845 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 31722-845. 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.