augmentin es-600

Generic: amoxicillin and clavulanate potassium

Labeler: usantibiotics, llc
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name augmentin es-600
Generic Name amoxicillin and clavulanate potassium
Labeler usantibiotics, llc
Dosage Form FOR SUSPENSION
Routes
ORAL
Active Ingredients

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

Manufacturer
USAntibiotics, LLC

Identifiers & Regulatory

Product NDC 81964-003
Product ID 81964-003_c310871a-ee00-42f4-b846-cd12cebc39bd
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA050755
Listing Expiration 2026-12-31
Marketing Start 2022-07-15

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 81964003
Hyphenated Format 81964-003

Supplemental Identifiers

RxCUI
617993 618028
UPC
0381964003697 0381964003543
UNII
804826J2HU Q42OMW3AT8

Packaging Origin

Original Packager
true

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 augmentin es-600 (source: ndc)
Generic Name amoxicillin and clavulanate potassium (source: ndc)
Application Number NDA050755 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 600 mg/5mL
  • 42.9 mg/5mL
source: ndc
Packaging
  • 75 mL in 1 BOTTLE (81964-003-51)
  • 200 mL in 1 BOTTLE (81964-003-54)
  • 125 mL in 1 BOTTLE (81964-003-69)
source: ndc

Packages (3)

81964-003-51 75 mL in 1 BOTTLE (81964-003-51) 81964-003-54 200 mL in 1 BOTTLE (81964-003-54) 81964-003-69 125 mL in 1 BOTTLE (81964-003-69)

Ingredients (2)

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

Linked Drug Pages (1)

AUGMENTIN ES-600 ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "c310871a-ee00-42f4-b846-cd12cebc39bd", "openfda": {"upc": ["0381964003697", "0381964003543"], "unii": ["804826J2HU", "Q42OMW3AT8"], "rxcui": ["617993", "618028"], "spl_set_id": ["59979859-8c9b-4173-a5e3-2e6312fd9d79"], "manufacturer_name": ["USAntibiotics, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "75 mL in 1 BOTTLE (81964-003-51)", "package_ndc": "81964-003-51", "marketing_start_date": "20220715"}, {"sample": false, "description": "200 mL in 1 BOTTLE (81964-003-54)", "package_ndc": "81964-003-54", "marketing_start_date": "20220715"}, {"sample": false, "description": "125 mL in 1 BOTTLE (81964-003-69)", "package_ndc": "81964-003-69", "marketing_start_date": "20220715"}], "brand_name": "AUGMENTIN ES-600", "product_id": "81964-003_c310871a-ee00-42f4-b846-cd12cebc39bd", "dosage_form": "FOR SUSPENSION", "pharm_class": ["Penicillin-class Antibacterial [EPC]", "Penicillins [CS]", "beta Lactamase Inhibitor [EPC]", "beta Lactamase Inhibitors [MoA]"], "product_ndc": "81964-003", "generic_name": "amoxicillin and clavulanate potassium", "labeler_name": "USAntibiotics, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "AUGMENTIN ES-600", "active_ingredients": [{"name": "AMOXICILLIN", "strength": "600 mg/5mL"}, {"name": "CLAVULANATE POTASSIUM", "strength": "42.9 mg/5mL"}], "application_number": "NDA050755", "marketing_category": "NDA", "marketing_start_date": "20220715", "listing_expiration_date": "20261231"}