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
50090-6381
Product ID
50090-6381_63491821-5b94-4a6a-bf52-6a7ba556cabc
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA065098
Listing Expiration
2026-12-31
Marketing Start
2004-08-13
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
500906381
Hyphenated Format
50090-6381
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
ANDA065098 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 400 mg/5mL
- 57 mg/5mL
Packaging
- 50 mL in 1 BOTTLE (50090-6381-0)
Packages (1)
Ingredients (2)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "63491821-5b94-4a6a-bf52-6a7ba556cabc", "openfda": {"unii": ["804826J2HU", "Q42OMW3AT8"], "rxcui": ["617430"], "spl_set_id": ["029a49f2-2132-4160-a0d6-2d108a456a22"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "50 mL in 1 BOTTLE (50090-6381-0)", "package_ndc": "50090-6381-0", "marketing_start_date": "20230227"}], "brand_name": "Amoxicillin and Clavulanate Potassium", "product_id": "50090-6381_63491821-5b94-4a6a-bf52-6a7ba556cabc", "dosage_form": "POWDER, FOR SUSPENSION", "pharm_class": ["Penicillin-class Antibacterial [EPC]", "Penicillins [CS]", "beta Lactamase Inhibitor [EPC]", "beta Lactamase Inhibitors [MoA]"], "product_ndc": "50090-6381", "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": "ANDA065098", "marketing_category": "ANDA", "marketing_start_date": "20040813", "listing_expiration_date": "20261231"}