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
Routes
ORAL
Active Ingredients

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

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-3179
Product ID 50090-3179_2694cd89-604e-4636-b516-d4569d1e4c29
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA203824
Listing Expiration 2027-12-31
Marketing Start 2016-08-23

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 500903179
Hyphenated Format 50090-3179

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 ANDA203824 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 875 mg/1
  • 125 mg/1
source: ndc
Packaging
  • 20 TABLET in 1 BOTTLE (50090-3179-0)
  • 10 TABLET in 1 BOTTLE (50090-3179-1)
  • 14 TABLET in 1 BOTTLE (50090-3179-2)
  • 28 TABLET in 1 BOTTLE (50090-3179-3)
source: ndc

Packages (4)

50090-3179-0 20 TABLET in 1 BOTTLE (50090-3179-0) 50090-3179-1 10 TABLET in 1 BOTTLE (50090-3179-1) 50090-3179-2 14 TABLET in 1 BOTTLE (50090-3179-2) 50090-3179-3 28 TABLET in 1 BOTTLE (50090-3179-3)

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": "2694cd89-604e-4636-b516-d4569d1e4c29", "openfda": {"unii": ["804826J2HU", "Q42OMW3AT8"], "rxcui": ["562508"], "spl_set_id": ["a3d1c0bb-94f3-4cfb-a4c6-233cf7e519a4"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET in 1 BOTTLE (50090-3179-0)", "package_ndc": "50090-3179-0", "marketing_start_date": "20171016"}, {"sample": false, "description": "10 TABLET in 1 BOTTLE (50090-3179-1)", "package_ndc": "50090-3179-1", "marketing_start_date": "20171222"}, {"sample": false, "description": "14 TABLET in 1 BOTTLE (50090-3179-2)", "package_ndc": "50090-3179-2", "marketing_start_date": "20171101"}, {"sample": false, "description": "28 TABLET in 1 BOTTLE (50090-3179-3)", "package_ndc": "50090-3179-3", "marketing_start_date": "20180329"}], "brand_name": "Amoxicillin and Clavulanate Potassium", "product_id": "50090-3179_2694cd89-604e-4636-b516-d4569d1e4c29", "dosage_form": "TABLET", "pharm_class": ["Penicillin-class Antibacterial [EPC]", "Penicillins [CS]", "beta Lactamase Inhibitor [EPC]", "beta Lactamase Inhibitors [MoA]"], "product_ndc": "50090-3179", "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": "ANDA203824", "marketing_category": "ANDA", "marketing_start_date": "20160823", "listing_expiration_date": "20271231"}