amoxicillin and clavulanate potassium
Generic: amoxicillin and clavulanate potassium
Labeler: a-s medication solutionsDrug 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
Active Ingredients
amoxicillin 400 mg/5mL, clavulanate potassium 57 mg/5mL
Manufacturer
Identifiers & Regulatory
Product NDC
50090-5873
Product ID
50090-5873_5ea4c6e7-0fff-4c6c-ae2f-e036637865f3
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA201090
Listing Expiration
2026-12-31
Marketing Start
2011-12-20
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
500905873
Hyphenated Format
50090-5873
Supplemental Identifiers
RxCUI
UNII
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
source: ndc
Resolved Composition
Strengths
- 400 mg/5mL
- 57 mg/5mL
Packaging
- 100 mL in 1 BOTTLE (50090-5873-0)
Packages (1)
Ingredients (2)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "5ea4c6e7-0fff-4c6c-ae2f-e036637865f3", "openfda": {"unii": ["804826J2HU", "Q42OMW3AT8"], "rxcui": ["617430"], "spl_set_id": ["2718248d-d948-466e-959b-1a972519f108"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "100 mL in 1 BOTTLE (50090-5873-0)", "package_ndc": "50090-5873-0", "marketing_start_date": "20211210"}], "brand_name": "Amoxicillin and Clavulanate Potassium", "product_id": "50090-5873_5ea4c6e7-0fff-4c6c-ae2f-e036637865f3", "dosage_form": "POWDER, FOR SUSPENSION", "pharm_class": ["Penicillin-class Antibacterial [EPC]", "Penicillins [CS]", "beta Lactamase Inhibitor [EPC]", "beta Lactamase Inhibitors [MoA]"], "product_ndc": "50090-5873", "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"}