amoxicillin and clavulanate potassium

Generic: amoxicillin and clavulanate potassium

Labeler: a-s medication solutions
NDC Directory HUMAN PRESCRIPTION DRUG NDA AUTHORIZED GENERIC 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, COATED
Routes
ORAL
Active Ingredients

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

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-6324
Product ID 50090-6324_a2a30785-599c-4436-a3cc-b4db011b7a87
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA AUTHORIZED GENERIC
Application Number NDA050720
Listing Expiration 2026-12-31
Marketing Start 2022-11-21

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 500906324
Hyphenated Format 50090-6324

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 NDA050720 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 875 mg/1
  • 125 mg/1
source: ndc
Packaging
  • 20 TABLET, COATED in 1 BOTTLE (50090-6324-0)
  • 10 TABLET, COATED in 1 BOTTLE (50090-6324-1)
  • 14 TABLET, COATED in 1 BOTTLE (50090-6324-2)
  • 28 TABLET, COATED in 1 BOTTLE (50090-6324-3)
source: ndc

Packages (4)

50090-6324-0 20 TABLET, COATED in 1 BOTTLE (50090-6324-0) 50090-6324-1 10 TABLET, COATED in 1 BOTTLE (50090-6324-1) 50090-6324-2 14 TABLET, COATED in 1 BOTTLE (50090-6324-2) 50090-6324-3 28 TABLET, COATED in 1 BOTTLE (50090-6324-3)

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": "a2a30785-599c-4436-a3cc-b4db011b7a87", "openfda": {"unii": ["804826J2HU", "Q42OMW3AT8"], "rxcui": ["562508"], "spl_set_id": ["00cf4429-e37c-4490-b22d-3cd796124296"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET, COATED in 1 BOTTLE (50090-6324-0)", "package_ndc": "50090-6324-0", "marketing_start_date": "20230112"}, {"sample": false, "description": "10 TABLET, COATED in 1 BOTTLE (50090-6324-1)", "package_ndc": "50090-6324-1", "marketing_start_date": "20230112"}, {"sample": false, "description": "14 TABLET, COATED in 1 BOTTLE (50090-6324-2)", "package_ndc": "50090-6324-2", "marketing_start_date": "20230112"}, {"sample": false, "description": "28 TABLET, COATED in 1 BOTTLE (50090-6324-3)", "package_ndc": "50090-6324-3", "marketing_start_date": "20230112"}], "brand_name": "AMOXICILLIN AND CLAVULANATE POTASSIUM", "product_id": "50090-6324_a2a30785-599c-4436-a3cc-b4db011b7a87", "dosage_form": "TABLET, COATED", "pharm_class": ["Penicillin-class Antibacterial [EPC]", "Penicillins [CS]", "beta Lactamase Inhibitor [EPC]", "beta Lactamase Inhibitors [MoA]"], "product_ndc": "50090-6324", "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": "NDA050720", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20221121", "listing_expiration_date": "20261231"}