0781-1852 : Amoxicillin (As Amoxicillin Trihydrate) 875 mg / Clavulanic Acid (As Clavulanate Potassium) 125 mg Oral Tablet


NDC0781-1852
Labeler: Sandoz Inc
Product Type: Human Prescription Drug
Drug Name:  Amoxicillin and Clavulanate Potassium
Dosage Form: Oral Tablet, Film Coated
Application #: ANDA065063
Rev. Date: 


Appearance:


Markings: GGN7
Shapes:  Oval
Colors:  White
Size (mm): 22
Segments: * 2

* Segments = the number of equally sized pieces which the pill can be broken into. In this case, a value of 2 indicates a scored pill which can be broken into 2 equal pieces.

GGN7: (0781-1852) Amoxicillin (As Amoxicillin Trihydrate) 875 mg / Clavulanic Acid (As Clavulanate Potassium) 125 mg Oral Tablet by Sandoz Inc
The above image is provided by the U.S. National Library of Medicine (NLM) and is not part of the official label.

NDC Package Codes:

  • 0781-1852-01: 100 TABLET, FILM COATED IN 1 BOTTLE (0781‑1852‑01)
  • 0781-1852-13: 100 TABLET, FILM COATED IN 1 BOX, UNIT‑DOSE (0781‑1852‑13)
  • 0781-1852-20: 20 TABLET, FILM COATED IN 1 BOTTLE (0781‑1852‑20)

Active Ingredients:

  • Amoxicillin
  • Clavulanate Potassium

Dosage Strength:

  • 875 mg
  • 125 mg

Inactive Ingredients:

  • Cellulose, Microcrystalline
  • Cetyl Alcohol
  • Crospovidone
  • Ethylcelluloses
  • Hypromelloses
  • Magnesium Stearate
  • Silicon Dioxide
  • Sodium Lauryl Sulfate
  • Sodium Starch Glycolate Type a Potato
  • Talc
  • Titanium Dioxide
  • Triethyl Citrate

Pharmaceutical Classes:

  • Penicillin-class Antibacterial [EPC]
  • Penicillins [CS]
  • beta Lactamase Inhibitor [EPC]
  • beta Lactamase Inhibitors [MoA]

Related Products:

Based on records with the same trade name.
  • 0781-1619 Amoxicillin 200 mg / Clavulanate 28.5 mg Chewable Tablet by Sandoz Inc
  • 0781-1643 Amoxicillin 400 mg / Clavulanate 57 mg Chewable Tablet by Sandoz Inc
  • 0781-1831 Amoxicillin (As Amoxicillin Trihydrate) 500 mg / Clavulanic Acid (As Clavulanate Potassium) 125 mg Oral Tablet by Sandoz Inc
  • 0781-1874 Amoxicillin (As Amoxicillin Trihydrate) 250 mg / Clavulanic Acid (As Clavulanate Potassium) 125 mg Oral Tablet by Sandoz Inc
  • 0781-1943 Amoxicillin 1000 mg / Clavulanate 62.5 mg 12 Hr Extended Release Tablet by Sandoz Inc
  • 0781-6102 Amoxicillin and Clavulanate Potassium Oral Powder, for Suspension by Sandoz Inc
  • 0781-6104 Amoxicillin and Clavulanate Potassium Oral Powder, for Suspension by Sandoz Inc
  • 0781-6139 Amoxicillin and Clavulanate Potassium Oral Suspension by Sandoz Inc
  • 66685-1001 Amoxicillin (As Amoxicillin Trihydrate) 875 mg / Clavulanic Acid (As Clavulanate Potassium) 125 mg Oral Tablet by Sandoz Inc
  • 66685-1002 Amoxicillin (As Amoxicillin Trihydrate) 500 mg / Clavulanic Acid (As Clavulanate Potassium) 125 mg Oral Tablet by Sandoz Inc
  • 66685-1011 Amoxicillin and Clavulanate Potassium Oral Powder, for Suspension by Sandoz Inc
  • 66685-1012 Amoxicillin and Clavulanate Potassium Oral Powder, for Suspension by Sandoz Inc
  • 0093-2270 Amoxicillin 200 mg / Clavulanate 28.5 mg Chewable Tablet by Teva Pharmaceuticals USA Inc
  • 0093-2272 Amoxicillin 400 mg / Clavulanate 57 mg Chewable Tablet by Teva Pharmaceuticals USA Inc
  • 0093-2274 Amoxicillin (As Amoxicillin Trihydrate) 500 mg / Clavulanic Acid (As Clavulanate Potassium) 125 mg Oral Tablet by Teva Pharmaceuticals USA Inc
  • 0093-2275 Amoxicillin (As Amoxicillin Trihydrate) 875 mg / Clavulanic Acid (As Clavulanate Potassium) 125 mg Oral Tablet by Teva Pharmaceuticals USA Inc
  • 0093-2277 Amoxicillin and Clavulanate Potassium Oral Powder, for Suspension by Teva Pharmaceuticals USA Inc
  • 0093-2279 Amoxicillin and Clavulanate Potassium Oral Powder, for Suspension by Teva Pharmaceuticals USA Inc
  • 0093-8675 Amoxicillin and Clavulanate Potassium Oral Powder, for Suspension by Teva Pharmaceuticals USA Inc
  • 0143-9249 Amoxicillin and Clavulanate Potassium Oral Tablet by West-ward Pharmaceuticals Corp
  • More related products ...

NDC QR Code

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NDC 0781-1852 QR Code

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Note: The RxChat NDC Database uses publicly available data from the FDA and the U.S. National Library of Medicine (NLM); The NLM is not responsible for the data presented and does not endorse or recommend this or any other product. While we make every effort to ensure that the information presented is accurate, you should assume that all results are unvalidated. To report any errors or inconsistencies please contact us.