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PACK IN HAND · ONE-PAGE CHECK

Medicine pack check sheet

Print this sheet or fill it in before speaking with a pharmacist or clinician. Copy only what is printed on the pack in hand. The published fields below are starting points from this record, not proof that your pack is the same product.

Published record starting point

Record display name
Avelox
Generic name / active ingredient
moxifloxacin
Dosage-form class
Dosage form and presentation as documented in the linked primary label
Route
Oral
Record reviewed
2026-08-25

Copy from the pack in hand

Source-linked reading points

  • First check AVELOX, moxifloxacin, 400 mg, oral tablet and target market together. 400 mg is an identity field for that oral tablet, not an answer to how many tablets anyone should use today, for how long, or whether leftovers can be continued.
  • The same FDA file also lists an intravenous product. Oral tablets and intravenous infusions differ in dosage form, route and handling requirements; intravenous-bag wording, oral-tablet numbers and another moxifloxacin or fluoroquinolone product must not be converted across one another.
  • The FDA label includes warnings about serious fluoroquinolone reactions, heart-rhythm risk and interactions. With acute or serious symptoms such as tendon pain or swelling, numbness or tingling, marked neurologic or mental-status change, palpitations or fainting, breathing difficulty, rash, or swelling of the face or mouth, use timely local medical support rather than switching to another antibacterial medicine or continuing based on a webpage.
  • Whether an antibacterial medicine is needed, which one is selected, route and course must be determined from the specific infection, testing, individual circumstances, complete medicine list and current target-market label. Especially with products that affect heart rhythm, glucose or anticoagulation, mineral-containing supplements, or multiple prescription/OTC products, bring the actual pack to a clinician or pharmacist for review.

Reviewed presentation examples — compare every field

  • 400 mg per tablet; 30-tablet bottle (U.S. historical label)NDC 50419-530-01

EDITORIAL RECORD

Who prepared and checked this page

Byline
OriginDrug Content Editorial
Review role
Public primary-source verification
Last reviewed
2026-08-25
Source record
2 clickable primary-source entry points are listed with this dossier.

The review role checks source traceability, stated market, document version and product-identity fields. It is not a claim of clinical licensure, prescribing authority or individual pharmacy service. Read the editorial policy.

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