amoxicillin
Generic: amoxicillin
Labeler: a-s medication solutionsDrug Facts
Product Profile
Brand Name
amoxicillin
Generic Name
amoxicillin
Labeler
a-s medication solutions
Dosage Form
TABLET, COATED
Routes
Active Ingredients
amoxicillin 875 mg/1
Manufacturer
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
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
500905880
Hyphenated Format
50090-5880
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 (source: ndc)
Generic Name
amoxicillin (source: ndc)
Application Number
ANDA065255 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 875 mg/1
Packaging
- 20 TABLET, COATED in 1 BOTTLE (50090-5880-0)
- 14 TABLET, COATED in 1 BOTTLE (50090-5880-1)
Packages (2)
Ingredients (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"}