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Moxifloxacin

NDC 33342-322, Moxifloxacin, tablet, film coated, from Macleods Pharmaceuticals Limited.

Product NDC
33342-322
Status
Listed
Labeler
Macleods Pharmaceuticals Limited
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA209143
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/33342-322 \
  -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
33342-322-073334203220730 TABLET, FILM COATED in 1 BOTTLE (33342-322-07)
33342-322-123334203221210 BLISTER PACK in 1 CARTON (33342-322-12) / 10 TABLET, FILM COATED in 1 BLISTER PACK

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/182ecd0f-714f-42f0-9b16-fb604cf15786

Use it

Look up 33342-322 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/33342-322 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 33342-322. 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.