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 POWDER, FOR SUSPENSION
Routes
ORAL
Active Ingredients

amoxicillin 125 mg/5mL

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-0404
Product ID 50090-0404_a0cc68fb-42ca-4ef3-8e6e-a75952096a13
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA065322
Listing Expiration 2026-12-31
Marketing Start 2006-06-19

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 500900404
Hyphenated Format 50090-0404

Supplemental Identifiers

RxCUI
313797
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 ANDA065322 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 125 mg/5mL
source: ndc
Packaging
  • 100 mL in 1 BOTTLE (50090-0404-0)
source: ndc

Packages (1)

50090-0404-0 100 mL in 1 BOTTLE (50090-0404-0)

Ingredients (1)

amoxicillin (125 mg/5mL)

Linked Drug Pages (1)

Amoxicillin ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "a0cc68fb-42ca-4ef3-8e6e-a75952096a13", "openfda": {"unii": ["804826J2HU"], "rxcui": ["313797"], "spl_set_id": ["60c7ae87-9631-4b29-9ca4-82fb3bafcab8"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "100 mL in 1 BOTTLE (50090-0404-0)", "package_ndc": "50090-0404-0", "marketing_start_date": "20160629"}], "brand_name": "Amoxicillin", "product_id": "50090-0404_a0cc68fb-42ca-4ef3-8e6e-a75952096a13", "dosage_form": "POWDER, FOR SUSPENSION", "pharm_class": ["Penicillin-class Antibacterial [EPC]", "Penicillins [CS]"], "product_ndc": "50090-0404", "generic_name": "Amoxicillin", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amoxicillin", "active_ingredients": [{"name": "AMOXICILLIN", "strength": "125 mg/5mL"}], "application_number": "ANDA065322", "marketing_category": "ANDA", "marketing_start_date": "20060619", "listing_expiration_date": "20261231"}