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, FILM COATED
Routes
ORAL
Active Ingredients

amoxicillin 875 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-0714
Product ID 50090-0714_156fa79e-91a6-460c-8f93-af5115b9588a
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA065256
Listing Expiration 2026-12-31
Marketing Start 2005-11-09

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 500900714
Hyphenated Format 50090-0714

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 ANDA065256 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 875 mg/1
source: ndc
Packaging
  • 20 TABLET, FILM COATED in 1 BOTTLE (50090-0714-0)
  • 14 TABLET, FILM COATED in 1 BOTTLE (50090-0714-1)
source: ndc

Packages (2)

50090-0714-0 20 TABLET, FILM COATED in 1 BOTTLE (50090-0714-0) 50090-0714-1 14 TABLET, FILM COATED in 1 BOTTLE (50090-0714-1)

Ingredients (1)

amoxicillin (875 mg/1)

Linked Drug Pages (1)

Amoxicillin ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "156fa79e-91a6-460c-8f93-af5115b9588a", "openfda": {"unii": ["804826J2HU"], "rxcui": ["308194"], "spl_set_id": ["00fbd46e-05fd-4f8a-9f59-a7a4d01c8e54"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE (50090-0714-0)", "package_ndc": "50090-0714-0", "marketing_start_date": "20141128"}, {"sample": false, "description": "14 TABLET, FILM COATED in 1 BOTTLE (50090-0714-1)", "package_ndc": "50090-0714-1", "marketing_start_date": "20231214"}], "brand_name": "Amoxicillin", "product_id": "50090-0714_156fa79e-91a6-460c-8f93-af5115b9588a", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Penicillin-class Antibacterial [EPC]", "Penicillins [CS]"], "product_ndc": "50090-0714", "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": "ANDA065256", "marketing_category": "ANDA", "marketing_start_date": "20051109", "listing_expiration_date": "20261231"}