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 POWDER, FOR SUSPENSION
Routes
ORAL
Active Ingredients

amoxicillin 400 mg/5mL, clavulanate potassium 57 mg/5mL

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-6694
Product ID 50090-6694_d80d6048-219c-4fbf-ac8c-432993ff9b95
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA201090
Listing Expiration 2026-12-31
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 500906694
Hyphenated Format 50090-6694

Supplemental Identifiers

RxCUI
617430
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 ANDA201090 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 400 mg/5mL
  • 57 mg/5mL
source: ndc
Packaging
  • 50 mL in 1 BOTTLE (50090-6694-0)
source: ndc

Packages (1)

50090-6694-0 50 mL in 1 BOTTLE (50090-6694-0)

Ingredients (2)

amoxicillin (400 mg/5mL) clavulanate potassium (57 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": "d80d6048-219c-4fbf-ac8c-432993ff9b95", "openfda": {"unii": ["804826J2HU", "Q42OMW3AT8"], "rxcui": ["617430"], "spl_set_id": ["ce488c24-2ec5-4d1b-b446-90f2497aa15d"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "50 mL in 1 BOTTLE (50090-6694-0)", "package_ndc": "50090-6694-0", "marketing_start_date": "20230918"}], "brand_name": "Amoxicillin and Clavulanate Potassium", "product_id": "50090-6694_d80d6048-219c-4fbf-ac8c-432993ff9b95", "dosage_form": "POWDER, FOR SUSPENSION", "pharm_class": ["Penicillin-class Antibacterial [EPC]", "Penicillins [CS]", "beta Lactamase Inhibitor [EPC]", "beta Lactamase Inhibitors [MoA]"], "product_ndc": "50090-6694", "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": "400 mg/5mL"}, {"name": "CLAVULANATE POTASSIUM", "strength": "57 mg/5mL"}], "application_number": "ANDA201090", "marketing_category": "ANDA", "marketing_start_date": "20111220", "listing_expiration_date": "20261231"}