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 250 mg/5mL

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-6469
Product ID 50090-6469_94dbe808-3c56-4d9c-9243-0647165bd692
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA204030
Listing Expiration 2026-12-31
Marketing Start 2014-09-15

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 500906469
Hyphenated Format 50090-6469

Supplemental Identifiers

RxCUI
239191
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 ANDA204030 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 250 mg/5mL
source: ndc
Packaging
  • 80 mL in 1 BOTTLE (50090-6469-0)
source: ndc

Packages (1)

50090-6469-0 80 mL in 1 BOTTLE (50090-6469-0)

Ingredients (1)

amoxicillin (250 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": "94dbe808-3c56-4d9c-9243-0647165bd692", "openfda": {"unii": ["804826J2HU"], "rxcui": ["239191"], "spl_set_id": ["efc66d77-1733-41e1-9aed-7c10a4b4ba96"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "80 mL in 1 BOTTLE (50090-6469-0)", "package_ndc": "50090-6469-0", "marketing_start_date": "20230508"}], "brand_name": "Amoxicillin", "product_id": "50090-6469_94dbe808-3c56-4d9c-9243-0647165bd692", "dosage_form": "POWDER, FOR SUSPENSION", "pharm_class": ["Penicillin-class Antibacterial [EPC]", "Penicillins [CS]"], "product_ndc": "50090-6469", "generic_name": "Amoxicillin", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amoxicillin", "active_ingredients": [{"name": "AMOXICILLIN", "strength": "250 mg/5mL"}], "application_number": "ANDA204030", "marketing_category": "ANDA", "marketing_start_date": "20140915", "listing_expiration_date": "20261231"}