amoxicillin

Generic: amoxicillin

Labeler: teva pharmaceuticals usa, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name amoxicillin
Generic Name amoxicillin
Labeler teva pharmaceuticals usa, inc.
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

amoxicillin 875 mg/1

Manufacturer
Teva Pharmaceuticals USA, Inc.

Identifiers & Regulatory

Product NDC 0093-2264
Product ID 0093-2264_31223839-1653-4906-826a-f9d6af179334
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA065056
Listing Expiration 2026-12-31
Marketing Start 2000-09-26

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 00932264
Hyphenated Format 0093-2264

Supplemental Identifiers

RxCUI
239191 308177 308182 308189 308191 308192 308194 313850 598025
UPC
0300933107051 0300932264014 0300934161731 0300933109055 0300932267015 0300932268012 0300932263017 0300934160734 0300934155730
UNII
804826J2HU

Packaging Origin

Original Packager
true

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 ANDA065056 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 875 mg/1
source: ndc
Packaging
  • 100 TABLET, FILM COATED in 1 BOTTLE (0093-2264-01)
source: ndc

Packages (1)

0093-2264-01 100 TABLET, FILM COATED in 1 BOTTLE (0093-2264-01)

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": "31223839-1653-4906-826a-f9d6af179334", "openfda": {"upc": ["0300933107051", "0300932264014", "0300934161731", "0300933109055", "0300932267015", "0300932268012", "0300932263017", "0300934160734", "0300934155730"], "unii": ["804826J2HU"], "rxcui": ["239191", "308177", "308182", "308189", "308191", "308192", "308194", "313850", "598025"], "spl_set_id": ["4c0f348a-a65d-409c-8668-207c82a5e3cb"], "manufacturer_name": ["Teva Pharmaceuticals USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (0093-2264-01)", "package_ndc": "0093-2264-01", "marketing_start_date": "20000926"}], "brand_name": "Amoxicillin", "product_id": "0093-2264_31223839-1653-4906-826a-f9d6af179334", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Penicillin-class Antibacterial [EPC]", "Penicillins [CS]"], "product_ndc": "0093-2264", "generic_name": "Amoxicillin", "labeler_name": "Teva Pharmaceuticals USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amoxicillin", "active_ingredients": [{"name": "AMOXICILLIN", "strength": "875 mg/1"}], "application_number": "ANDA065056", "marketing_category": "ANDA", "marketing_start_date": "20000926", "listing_expiration_date": "20261231"}