amoxicillin and clavulanate potassium (50090-2219)

Drug Facts

Product Profile

Brand Name amoxicillin and clavulanate potassium

Generic Name amoxicillin and clavulanate potassium

Labeler a-s medication solutions

Dosage Form POWDER, FOR SUSPENSION

Routes

ORAL

Active Ingredients

amoxicillin 600 mg/5mL, clavulanate potassium 42.9 mg/5mL

Manufacturer

A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-2219

Product ID 50090-2219_8a5c825a-50d7-4797-a7f3-8a61758c0c4e

Product Type HUMAN PRESCRIPTION DRUG

Marketing Category ANDA

Application Number ANDA201091

Listing Expiration 2027-12-31

Marketing Start 2011-12-20

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 500902219

Hyphenated Format 50090-2219

Supplemental Identifiers

RxCUI

617993

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 ANDA201091 (source: ndc)

Routes

ORAL

source: ndc

Resolved Composition

Strengths

600 mg/5mL
42.9 mg/5mL

source: ndc

Packaging

125 mL in 1 BOTTLE (50090-2219-0)

source: ndc

Packages (1)

50090-2219-0 125 mL in 1 BOTTLE (50090-2219-0)

Ingredients (2)

amoxicillin (600 mg/5mL) clavulanate potassium (42.9 mg/5mL)

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": "8a5c825a-50d7-4797-a7f3-8a61758c0c4e", "openfda": {"unii": ["804826J2HU", "Q42OMW3AT8"], "rxcui": ["617993"], "spl_set_id": ["2a376d67-0bf2-43a1-8ca3-73f90689c339"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "125 mL in 1 BOTTLE (50090-2219-0)", "package_ndc": "50090-2219-0", "marketing_start_date": "20151106"}], "brand_name": "Amoxicillin and Clavulanate Potassium", "product_id": "50090-2219_8a5c825a-50d7-4797-a7f3-8a61758c0c4e", "dosage_form": "POWDER, FOR SUSPENSION", "pharm_class": ["Penicillin-class Antibacterial [EPC]", "Penicillins [CS]", "beta Lactamase Inhibitor [EPC]", "beta Lactamase Inhibitors [MoA]"], "product_ndc": "50090-2219", "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": "600 mg/5mL"}, {"name": "CLAVULANATE POTASSIUM", "strength": "42.9 mg/5mL"}], "application_number": "ANDA201091", "marketing_category": "ANDA", "marketing_start_date": "20111220", "listing_expiration_date": "20271231"}