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Moxifloxacin Hydrochloride

NDC 68084-722, Moxifloxacin Hydrochloride, tablet, film coated, from American Health Packaging.

Product NDC
68084-722
Status
Listed
Labeler
American Health Packaging
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/68084-722 \
  -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
68084-722-656808407226550 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-722-65) / 1 TABLET, FILM COATED in 1 BLISTER PACK (68084-722-11)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/1ed191f5-7df5-488c-bb72-91ac0b618d9a

  • NADAC price for package 68084072265

    GET /v1/drugs/nadac/68084072265

Use it

Look up 68084-722 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68084-722 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68084-722. 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.