amoxicillin

Generic: amoxicillin

Labeler: a-s medication solutions
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name amoxicillin
Generic Name amoxicillin
Labeler a-s medication solutions
Dosage Form TABLET, COATED
Routes
ORAL
Active Ingredients

amoxicillin 875 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-5880
Product ID 50090-5880_33b6a1ef-8834-4091-9d82-a36696ae7ad6
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA065255
Listing Expiration 2026-12-31
Marketing Start 2006-03-29

Pharmacologic Class

Classes
penicillin-class antibacterial [epc] penicillins [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 500905880
Hyphenated Format 50090-5880

Supplemental Identifiers

RxCUI
308194
UNII
804826J2HU

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 (source: ndc)
Generic Name amoxicillin (source: ndc)
Application Number ANDA065255 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 875 mg/1
source: ndc
Packaging
  • 20 TABLET, COATED in 1 BOTTLE (50090-5880-0)
  • 14 TABLET, COATED in 1 BOTTLE (50090-5880-1)
source: ndc

Packages (2)

Ingredients (1)

amoxicillin (875 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "33b6a1ef-8834-4091-9d82-a36696ae7ad6", "openfda": {"unii": ["804826J2HU"], "rxcui": ["308194"], "spl_set_id": ["85721bc3-37eb-4db6-8a40-8a1412ac953a"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET, COATED in 1 BOTTLE (50090-5880-0)", "package_ndc": "50090-5880-0", "marketing_start_date": "20211221"}, {"sample": false, "description": "14 TABLET, COATED in 1 BOTTLE (50090-5880-1)", "package_ndc": "50090-5880-1", "marketing_start_date": "20240816"}], "brand_name": "Amoxicillin", "product_id": "50090-5880_33b6a1ef-8834-4091-9d82-a36696ae7ad6", "dosage_form": "TABLET, COATED", "pharm_class": ["Penicillin-class Antibacterial [EPC]", "Penicillins [CS]"], "product_ndc": "50090-5880", "generic_name": "Amoxicillin", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amoxicillin", "active_ingredients": [{"name": "AMOXICILLIN", "strength": "875 mg/1"}], "application_number": "ANDA065255", "marketing_category": "ANDA", "marketing_start_date": "20060329", "listing_expiration_date": "20261231"}