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Amoxicillin 500 mg and Clavulanate Potassium 100 mg for Injection

NAFDAC Reg. No. C4-1211 · Drug

Registered with NAFDAC — registration activeAs of 5 November 2026 · synced automatically from official sources.
Product
Amoxicillin 500 mg and Clavulanate Potassium 100 mg for Injection
NAFDAC number
C4-1211
Active ingredient
Amoxicillin (Amoxicillin Sodium); Clavulanic Acid (Potassium Clavulanate)
Strength
500 mg; 100 mg
Form
Powder for injection
Manufacturer
Not listed
Applicant (holder)
Geneith Pharmaceuticals Limited
Approved
10 Nov 2020
Status
Inactive View on NAFDAC ↗
Registration valid to
9 Nov 2025
WHO alerts
None found
Community reports
None
Times checked
0
Used to treat certain bacterial infections. General information only — antibiotics should only be used as prescribed by a doctor, and a full course should be completed.

RxVerify commentary

  • Amoxicillin 500 mg and Clavulanate Potassium 100 mg for Injection is on the NAFDAC register with an active registration (C4-1211). A valid number alone does not prove a pack is genuine — counterfeiters copy real numbers, so also check the expiry date, seal and print quality.

Generated automatically from the NAFDAC register, WHO alerts and community data as of today. Not medical advice — always follow your doctor or pharmacist.

What Amoxicillin 500 mg and Clavulanate Potassium 100 mg for Injection is used for

From the official U.S. FDA label for amoxicillin (amoxicillin sodium), the active ingredient registered with NAFDAC.

What it is used for

Adults and Pediatric Patients Upper Respiratory Tract Infections of the Ear, Nose, and Throat: Amoxicillin tablets are indicated in the treatment of infections due to susceptible (ONLY β-lactamase-negative) isolates of Streptococcus species. (α- and β-hemolytic isolates only), Streptococcus pneumoniae , Staphylococcus spp., or Haemophilus influenzae . Infections of the Genitourinary Tract: Amoxicillin tablets are indicated in the treatment of infections due to susceptible (ONLY β-lactamase–negative) isolates of Escherichia coli, Proteus mirabilis , or Enterococcus faecalis . …

Possible side effects

The following are discussed in more detail in other sections of the labeling: Anaphylactic reactions [see Warnings and Precautions (5.1) ] Severe Cutaneous Adverse Reactions [see Warnings and Precautions (5.2) ] Clostridioides difficile- Associated Diarrhea (CDAD) [see Warnings and Precautions (5.3) ] The most common adverse reactions (greater than 1%) observed in clinical trials of amoxicillin tablets or for oral suspension were diarrhea, rash, vomiting, and nausea. (6.1) To report SUSPECTED ADVERSE REACTIONS, contact Aurobindo Pharma USA, Inc. at 1-866-850-2876 or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch . …

Do not use if

Amoxicillin tablets are contraindicated in patients who have experienced a serious hypersensitivity reaction (e.g., anaphylaxis or Stevens-Johnson syndrome) to amoxicillin tablets or to other β-lactam antibacterial drugs (e.g., penicillins and cephalosporins). History of a serious hypersensitivity reaction (e.g., anaphylaxis or Stevens-Johnson syndrome) to amoxicillin tablets or to other beta-lactams (e.g., penicillins or cephalosporins). (4)

Warnings

Anaphylactic reactions: Serious and occasionally fatal anaphylactic reactions have been reported in patients on penicillin therapy, including amoxicillin. Discontinue amoxicillin if a reaction occurs ( 5.1 ). Severe cutaneous adverse reactions (SCAR): Monitor closely. Discontinue if rash progresses. ( 5.2 ) Clostridioides difficile -associated diarrhea (CDAD) (ranging from mild diarrhea to fatal colitis): Evaluate if diarrhea occurs. ( 5.3 ) 5.1 Anaphylactic Reactions Serious and occasionally fatal hypersensitivity (anaphylactic) reactions have been reported in patients on penicillin therapy including amoxicillin. …

Pregnancy & breastfeeding

8.1 Pregnancy Teratogenic Effects : Pregnancy Category B. Reproduction studies have been performed in mice and rats at doses up to 2000 mg/kg (3 and 6 times the 3 g human dose, based on body surface area). There was no evidence of harm to the fetus due to amoxicillin. There are, however, no adequate and well-controlled studies in pregnant women. …

General information only — not dosing advice. Always follow the leaflet in your pack and your doctor or pharmacist.

NAFDAC recall & alert notices

Public Alert No. 35/2025 – Substandard batches of Annmox (Amoxicillin suspensions 125mg/5ml) and Jawamox (Amoxicillin suspension 125mg/5ml) manufactured by Jawa International Ltd due to low Active Pharmaceutical Ingredient (API) content22 Oct 2025 · nafdac.gov.ngThe National Agency for Food and Drugs Administration and Control (NAFDAC) is notifying the public about the mop up of batches of confirmed substandard Annmox (Batch 360M) and Jawamox (Batch 4231M & 4290M) Suspensions.The products failed laboratory analysis due to low Active Pharmaceutical Ingredient (API) content.The …Public Alert No. 34/2025 –Substandard Astamocil (Amoxicillin Suspension 125mg/5ml), Batch No. 826024, and Astamentin (Amoxicillin/Clavulanic Acid Suspension), Batch Nos: 0503024 & 0501724, manufactured by Sam-Ace Ltd in Nigeria22 Oct 2025 · nafdac.gov.ngThe National Agency for Food and Drug Administration and Control (NAFDAC) is notifying the public about the recall of two products: Astamocil (Amoxicillin Suspension 125mg/5ml), Batch 826024, and Astamentin (Amoxicillin/Clavulanic Acid Suspension 228.5 mg), Batches 0503024 and 0501724, manufactured by Sam-Ace Ltd in Ni…Public Alert No. 024/2025 – Recall of Amoxivue (Amoxicillin) 500mg Capsules due to significantly low Active Pharmaceutical Ingredient (API) content6 Aug 2025 · nafdac.gov.ngThe National Agency for Food and Drug Administration and Control (NAFDAC) is alerting the public about the recall of Amoxivue (Amoxicillin) 500mg, with NAFDAC NO: A4-100178 and Batch NO: 322584, manufactured by Sparsh Bio-Tech Pvt, Ltd.Note: Sparsh Bio-Tech has declared no relationship with the MAH- MedVue Pharmaceutic…

Notices list affected brands and batch numbers — compare them with your pack. Enter your batch number above to check it automatically.

Check your pack of Amoxicillin 500 mg and Clavulanate Potassium 100 mg for Injection

Add the expiry date printed on your pack for a full Trust Score — or look up uses, side effects and cheaper generics.

3 free checks left today · no signup Official sources: NAFDAC Green Book & recalls · WHO · U.S. FDA · NLM RxNorm

About Amoxicillin 500 mg and Clavulanate Potassium 100 mg for Injection

What is in Amoxicillin 500 mg and Clavulanate Potassium 100 mg for Injection?

Amoxicillin 500 mg and Clavulanate Potassium 100 mg for Injection contains Amoxicillin (Amoxicillin Sodium); Clavulanic Acid (Potassium Clavulanate) (500 mg; 100 mg), as powder for injection, according to its NAFDAC registration record.

Is Amoxicillin 500 mg and Clavulanate Potassium 100 mg for Injection registered with NAFDAC?

Yes. Amoxicillin 500 mg and Clavulanate Potassium 100 mg for Injection is listed on the NAFDAC register under registration number C4-1211, and its registration is active as of 5 November 2026.

Has Amoxicillin 500 mg and Clavulanate Potassium 100 mg for Injection been flagged as fake or recalled?

No WHO falsified or substandard medical product alert currently matches Amoxicillin 500 mg and Clavulanate Potassium 100 mg for Injection in our automatically synced alert list.

How can I check that my pack of Amoxicillin 500 mg and Clavulanate Potassium 100 mg for Injection is genuine?

Run a free authenticity scan with the NAFDAC number C4-1211, your pack's expiry date and batch number to get a Trust Score, compare the pack with the NAFDAC record (ingredient, strength, form, manufacturer), and buy only from licensed pharmacies.

What is Amoxicillin 500 mg and Clavulanate Potassium 100 mg for Injection used for?

Adults and Pediatric Patients Upper Respiratory Tract Infections of the Ear, Nose, and Throat: Amoxicillin tablets are indicated in the treatment of infections due to susceptible (ONLY β-lactamase-negative) isolates of Streptococcus species. (α- and β-hemolytic isolates only), Streptococcus pneumoniae , Staphylococcus spp., or Haemophilus influenzae . Infections of the Genitourinary Tract: Amoxici (Summarised from the official U.S. FDA label for amoxicillin (amoxicillin sodium). Always follow your doctor or pharmacist.)

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