amoxicillin and clavulanate potassium

Generic: amoxicillin and clavulanate potassium

Labeler: teva pharmaceuticals usa, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name amoxicillin and clavulanate potassium
Generic Name amoxicillin and clavulanate potassium
Labeler teva pharmaceuticals usa, inc.
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

amoxicillin 875 mg/1, clavulanate potassium 125 mg/1

Manufacturer
Teva Pharmaceuticals USA, Inc.

Identifiers & Regulatory

Product NDC 0093-2275
Product ID 0093-2275_aaf9ce2f-41c3-489c-b5c1-f4f553d84854
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA065096
Listing Expiration 2026-12-31
Marketing Start 2002-10-31

Pharmacologic Class

Classes
penicillin-class antibacterial [epc] penicillins [cs] beta lactamase inhibitor [epc] beta lactamase inhibitors [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 00932275
Hyphenated Format 0093-2275

Supplemental Identifiers

RxCUI
562508 617296 617423 617430
UPC
0300932274341 0300932275348
UNII
Q42OMW3AT8 804826J2HU

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name amoxicillin and clavulanate potassium (source: ndc)
Generic Name amoxicillin and clavulanate potassium (source: ndc)
Application Number ANDA065096 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 875 mg/1
  • 125 mg/1
source: ndc
Packaging
  • 20 TABLET, FILM COATED in 1 BOTTLE (0093-2275-34)
source: ndc

Packages (1)

0093-2275-34 20 TABLET, FILM COATED in 1 BOTTLE (0093-2275-34)

Ingredients (2)

amoxicillin (875 mg/1) clavulanate potassium (125 mg/1)

Linked Drug Pages (1)

Amoxicillin and Clavulanate Potassium ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "aaf9ce2f-41c3-489c-b5c1-f4f553d84854", "openfda": {"upc": ["0300932274341", "0300932275348"], "unii": ["Q42OMW3AT8", "804826J2HU"], "rxcui": ["562508", "617296", "617423", "617430"], "spl_set_id": ["963e7bea-ff5d-420a-9cb2-e4aefb534b33"], "manufacturer_name": ["Teva Pharmaceuticals USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE (0093-2275-34)", "package_ndc": "0093-2275-34", "marketing_start_date": "20021031"}], "brand_name": "Amoxicillin and Clavulanate Potassium", "product_id": "0093-2275_aaf9ce2f-41c3-489c-b5c1-f4f553d84854", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Penicillin-class Antibacterial [EPC]", "Penicillins [CS]", "beta Lactamase Inhibitor [EPC]", "beta Lactamase Inhibitors [MoA]"], "product_ndc": "0093-2275", "generic_name": "Amoxicillin and Clavulanate Potassium", "labeler_name": "Teva Pharmaceuticals USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amoxicillin and Clavulanate Potassium", "active_ingredients": [{"name": "AMOXICILLIN", "strength": "875 mg/1"}, {"name": "CLAVULANATE POTASSIUM", "strength": "125 mg/1"}], "application_number": "ANDA065096", "marketing_category": "ANDA", "marketing_start_date": "20021031", "listing_expiration_date": "20261231"}