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Moxifloxacin Hydrochloride

NDC 71335-2815, Moxifloxacin Hydrochloride, tablet, film coated, from Bryant Ranch Prepack.

Product NDC
71335-2815
Status
Listed
Labeler
Bryant Ranch Prepack
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA202632
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/71335-2815 \
  -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
71335-2815-1713352815017 TABLET, FILM COATED in 1 BOTTLE (71335-2815-1)
71335-2815-27133528150210 TABLET, FILM COATED in 1 BOTTLE (71335-2815-2)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/ac8a81b9-2fed-412a-8c83-db8dee1061f6

Use it

Look up 71335-2815 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71335-2815 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71335-2815. 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.