Drugplain

Moxifloxacin Hydrochloride Tablets, 400 mg 400 mg/1

Moxifloxacin Hydrochloride Tablets, 400 mg · TABLET, FILM COATED · Novadoz Pharmaceuticals LLC

No Recall HistoryCurrently in Shortage
Plain English

Moxifloxacin Hydrochloride Tablets, 400 mg is a tablet, film coated containing moxifloxacin hydrochloride tablets, 400 mg at 400 mg/1, taken oral. Manufactured by Novadoz Pharmaceuticals LLC.

Key Facts

Brand Name
Moxifloxacin Hydrochloride Tablets, 400 mg
Generic Name
Moxifloxacin Hydrochloride Tablets, 400 mg
NDC Code (Product)
72205-001
Manufacturer
Novadoz Pharmaceuticals LLC
Strength
400 mg/1
Dosage Form
TABLET, FILM COATED
Route
ORAL
Marketing Status
Application #
ANDA208682
Marketing Start
07/21/2018

Recall History

No Recall History

Side Effects Reported to FDA

FDA FAERS database · These are reported events, not confirmed side effects

drug ineffective3 reports
condition aggravated1 reports
depersonalisation/derealisation disorder1 reports
disease progression1 reports
dizziness1 reports
electrocardiogram qt prolonged1 reports
empyema1 reports
epilepsy1 reports
pneumonia streptococcal1 reports

Frequently Asked Questions

What is Moxifloxacin Hydrochloride Tablets, 400 mg used for?

Moxifloxacin Hydrochloride Tablets, 400 mg contains Moxifloxacin Hydrochloride Tablets, 400 mg. It is a tablet, film coated taken oral. Consult your doctor for specific uses.

Is Moxifloxacin Hydrochloride Tablets, 400 mg a controlled substance?

Moxifloxacin Hydrochloride Tablets, 400 mg is not classified as a controlled substance by the DEA.

What is the generic name for Moxifloxacin Hydrochloride Tablets, 400 mg?

The generic name for Moxifloxacin Hydrochloride Tablets, 400 mg is Moxifloxacin Hydrochloride Tablets, 400 mg. There are no other listed brand versions of Moxifloxacin Hydrochloride Tablets, 400 mg.

What is the NDC code for Moxifloxacin Hydrochloride Tablets, 400 mg 400 mg/1?

The NDC (National Drug Code) for Moxifloxacin Hydrochloride Tablets, 400 mg 400 mg/1 is 72205-001, listed by Novadoz Pharmaceuticals LLC.

Product NDC

72205-001

Package NDC

72205-001-05

Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.

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