Amoxicillin, Clavulanate Potassium Chewable Tablet 200-28.5Mg Drug Medication Dosage Information
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Amoxicillin, Clavulanate Potassium: Chewable tablet (200-28.5mg)

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Amox/Clav 200-28.5mg Chw Tab

What is this Medicine?

AMOXICILLIN; CLAVULANIC ACID (a mox i SIL in; KLAV yoo lan ic AS id) is a penicillin antibiotic. It is used to treat certain kinds of bacterial infections. It It will not work for colds, flu, or other viral infections.

CVS Pharmacy Patient Statistics for Amoxicillin, Clavulanate Potassium: Chewable tablet(200-28.5mg)
Generic vs. Brand Name Usage*
*Brand contains same active ingredient but may not represent FDA-approved generic equivalent
Usage By Strength
In-Depth Information
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Amoxicillin/Clavulanate Potassium 200mg-28.5mg Chewable Tablet

NDC: 000932270
  • Prescription Required
  • Not a Controlled Drug
    (CSA Schedule)
  • FDA Approved




FDA approved for the following conditions:
Pneumonia, Impetigo, Cystitis, Skin And Skin Structure Infections, Urinary Tract Infection (UTI), Sinusitis, Otitis Media, Lower Respiratory Tract Infections, Community-acquired Pneumonia

Sometimes used for but not FDA approved for the following conditions:
Febrile Neutropenia, Pericoronitis, Dental Infection, Dentoalveolar Infection, Periodontitis, Actinomycotic Mycetoma, Melioidosis

Storage Information
Store at controlled room temperature (between 68 and 77 degrees F)
Amoxicillin/Clavulanate Potassium 200mg-28.5mg Chewable Tablet
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Reported Side Effects for Amoxicillin/Clavulanate Potassium 200mg-28.5mg Chewable Tablet

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High Platelet Count Incidence:
<1.0%*
Severity: MODERATE
Onset: DELAYED
Yeast Infection Incidence:
1.0-6.0%*
Severity: MODERATE
Onset: DELAYED
Skin Rash Incidence:
1.0-3.0%*
Severity: MILD
Onset: EARLY
Vomiting Incidence:
1.0-8.0%*
Severity: MILD
Onset: EARLY
Vaginal Infection Incidence:
1.0%*
Severity: MODERATE
Onset: DELAYED
Upset Stomach Incidence:
2.1-3.0%*
Severity: MILD
Onset: EARLY
Hives Incidence:
3.0%*
Severity: MILD
Onset: RAPID
Loose Stools Incidence:
4.0-34.3%*
Severity: MILD
Onset: EARLY
Diaper Rash Incidence:
5.0-6.0%*
Severity: MILD
Onset: DELAYED
*This is an approximate aggregated range of reported side effects from clinical studies performed on this drug. Your experience with this drug may be different.
Pregnancy & Lactation Information
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FIRST Trimester

Class B - Animal studies have revealed no evidence of harm to the fetus, however, there are no adequate and well-controlled studies in pregnant women. OR Animal studies have shown an adverse effect, but adequate and well-controlled studies in pregnant women have failed to demonstrate a risk to the fetus in any trimester.

SECOND Trimester

Class B - Animal studies have revealed no evidence of harm to the fetus, however, there are no adequate and well-controlled studies in pregnant women. OR Animal studies have shown an adverse effect, but adequate and well-controlled studies in pregnant women have failed to demonstrate a risk to the fetus in any trimester.

THIRD Trimester

Class B - Animal studies have revealed no evidence of harm to the fetus, however, there are no adequate and well-controlled studies in pregnant women. OR Animal studies have shown an adverse effect, but adequate and well-controlled studies in pregnant women have failed to demonstrate a risk to the fetus in any trimester.

Lactation

Compatible - This drug is generally safe to take by nursing mothers.


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