amoxicillin and clavulanate potassium (50090-6530)

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 50090-6530

Product ID 50090-6530_5b50becc-70fc-4266-ba5b-bc0770ad5fb5

Product Type HUMAN PRESCRIPTION DRUG

Marketing Category ANDA

Application Number ANDA065063

Marketing Start 2020-05-01

Marketing End 2026-06-30

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 500906530

Hyphenated Format 50090-6530

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 ANDA065063 (source: ndc)

Routes

ORAL

source: ndc

Resolved Composition

Strengths

875 mg/1
125 mg/1

source: ndc

Packaging

16 HOW SUPPLIED/STORAGE AND HANDLING Product: 50090-6530
Amoxicillin and Clavulanate Potassium Label Image

source: label

Packages (0)

No package records.

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": "5b50becc-70fc-4266-ba5b-bc0770ad5fb5", "openfda": {"unii": ["804826J2HU", "Q42OMW3AT8"], "rxcui": ["562508"], "spl_set_id": ["32906f4a-8b21-458d-b643-e6b1b0a8bb44"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [], "brand_name": "Amoxicillin and Clavulanate Potassium", "product_id": "50090-6530_5b50becc-70fc-4266-ba5b-bc0770ad5fb5", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Penicillin-class Antibacterial [EPC]", "Penicillins [CS]", "beta Lactamase Inhibitor [EPC]", "beta Lactamase Inhibitors [MoA]"], "product_ndc": "50090-6530", "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": "ANDA065063", "marketing_category": "ANDA", "marketing_end_date": "20260630", "marketing_start_date": "20200501"}