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Moxifloxacin

NDC 73473-903, moxifloxacin hydrochloride, tablet, film coated, from Solaris Pharma Corporation.

Product NDC
73473-903
Status
Listed
Labeler
Solaris Pharma Corporation
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA206295
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/73473-903 \
  -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
73473-903-307347309033030 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (73473-903-30)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/45ce14e5-98b8-296b-e063-6294a90a769b

  • NADAC price for package 73473090330

    GET /v1/drugs/nadac/73473090330

Use it

Look up 73473-903 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/73473-903 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 73473-903. 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.