amoxicillin and clavulanate potassium (50090-1809)

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 875 mg/1, clavulanate potassium 125 mg/1

Manufacturer

A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-1809

Product ID 50090-1809_d3ac1741-765a-4ffa-9a0b-b06a633ec88f

Product Type HUMAN PRESCRIPTION DRUG

Marketing Category ANDA

Application Number ANDA091568

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 500901809

Hyphenated Format 50090-1809

Supplemental Identifiers

RxCUI

562508

UNII

804826J2HU Q42OMW3AT8

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 ANDA091568 (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 (50090-1809-0)
10 TABLET, FILM COATED in 1 BOTTLE (50090-1809-1)
14 TABLET, FILM COATED in 1 BOTTLE (50090-1809-2)
28 TABLET, FILM COATED in 1 BOTTLE (50090-1809-3)

source: ndc

Packages (4)

50090-1809-0 20 TABLET, FILM COATED in 1 BOTTLE (50090-1809-0) 50090-1809-1 10 TABLET, FILM COATED in 1 BOTTLE (50090-1809-1) 50090-1809-2 14 TABLET, FILM COATED in 1 BOTTLE (50090-1809-2) 50090-1809-3 28 TABLET, FILM COATED in 1 BOTTLE (50090-1809-3)

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": "d3ac1741-765a-4ffa-9a0b-b06a633ec88f", "openfda": {"unii": ["804826J2HU", "Q42OMW3AT8"], "rxcui": ["562508"], "spl_set_id": ["924a9ef6-5e3d-4e78-ae97-ae090f6613c0"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE (50090-1809-0)", "package_ndc": "50090-1809-0", "marketing_start_date": "20150507"}, {"sample": false, "description": "10 TABLET, FILM COATED in 1 BOTTLE (50090-1809-1)", "package_ndc": "50090-1809-1", "marketing_start_date": "20250918"}, {"sample": false, "description": "14 TABLET, FILM COATED in 1 BOTTLE (50090-1809-2)", "package_ndc": "50090-1809-2", "marketing_start_date": "20150507"}, {"sample": false, "description": "28 TABLET, FILM COATED in 1 BOTTLE (50090-1809-3)", "package_ndc": "50090-1809-3", "marketing_start_date": "20150507"}], "brand_name": "Amoxicillin and Clavulanate Potassium", "product_id": "50090-1809_d3ac1741-765a-4ffa-9a0b-b06a633ec88f", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Penicillin-class Antibacterial [EPC]", "Penicillins [CS]", "beta Lactamase Inhibitor [EPC]", "beta Lactamase Inhibitors [MoA]"], "product_ndc": "50090-1809", "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": "875 mg/1"}, {"name": "CLAVULANATE POTASSIUM", "strength": "125 mg/1"}], "application_number": "ANDA091568", "marketing_category": "ANDA", "marketing_start_date": "20120120", "listing_expiration_date": "20261231"}