amoxicillin and clavulanate potassium

Generic: amoxicillin and clavulanate potassium

Labeler: a-s medication solutions
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 a-s medication solutions
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

amoxicillin 500 mg/1, clavulanate potassium 125 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-0820
Product ID 50090-0820_6dff41b3-f2fe-4f50-aef9-0b01bc06d458
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA091569
Listing Expiration 2026-12-31
Marketing Start 2012-01-20

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 500900820
Hyphenated Format 50090-0820

Supplemental Identifiers

RxCUI
562508 617296
UNII
Q42OMW3AT8 804826J2HU

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 ANDA091569 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 500 mg/1
  • 125 mg/1
source: ndc
Packaging
  • 20 TABLET, FILM COATED in 1 BOTTLE (50090-0820-0)
  • 21 TABLET, FILM COATED in 1 BOTTLE (50090-0820-1)
  • 30 TABLET, FILM COATED in 1 BOTTLE (50090-0820-2)
  • 15 TABLET, FILM COATED in 1 BOTTLE (50090-0820-3)
source: ndc

Packages (4)

50090-0820-0 20 TABLET, FILM COATED in 1 BOTTLE (50090-0820-0) 50090-0820-1 21 TABLET, FILM COATED in 1 BOTTLE (50090-0820-1) 50090-0820-2 30 TABLET, FILM COATED in 1 BOTTLE (50090-0820-2) 50090-0820-3 15 TABLET, FILM COATED in 1 BOTTLE (50090-0820-3)

Ingredients (2)

amoxicillin (500 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": "6dff41b3-f2fe-4f50-aef9-0b01bc06d458", "openfda": {"unii": ["Q42OMW3AT8", "804826J2HU"], "rxcui": ["562508", "617296"], "spl_set_id": ["af4c2ea8-73bd-429b-8392-fa20fec6fb3f"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE (50090-0820-0)", "package_ndc": "50090-0820-0", "marketing_start_date": "20141128"}, {"sample": false, "description": "21 TABLET, FILM COATED in 1 BOTTLE (50090-0820-1)", "package_ndc": "50090-0820-1", "marketing_start_date": "20141128"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (50090-0820-2)", "package_ndc": "50090-0820-2", "marketing_start_date": "20141128"}, {"sample": false, "description": "15 TABLET, FILM COATED in 1 BOTTLE (50090-0820-3)", "package_ndc": "50090-0820-3", "marketing_start_date": "20141128"}], "brand_name": "Amoxicillin and Clavulanate Potassium", "product_id": "50090-0820_6dff41b3-f2fe-4f50-aef9-0b01bc06d458", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Penicillin-class Antibacterial [EPC]", "Penicillins [CS]", "beta Lactamase Inhibitor [EPC]", "beta Lactamase Inhibitors [MoA]"], "product_ndc": "50090-0820", "generic_name": "Amoxicillin and Clavulanate Potassium", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amoxicillin and Clavulanate Potassium", "active_ingredients": [{"name": "AMOXICILLIN", "strength": "500 mg/1"}, {"name": "CLAVULANATE POTASSIUM", "strength": "125 mg/1"}], "application_number": "ANDA091569", "marketing_category": "ANDA", "marketing_start_date": "20120120", "listing_expiration_date": "20261231"}