amoxicillin

Generic: amoxicillin

Labeler: aurobindo pharma limited
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name amoxicillin
Generic Name amoxicillin
Labeler aurobindo pharma limited
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

amoxicillin 875 mg/1

Manufacturer
Aurobindo Pharma Limited

Identifiers & Regulatory

Product NDC 65862-015
Product ID 65862-015_ee0e12cd-e881-4048-a0fb-74bd771cb9aa
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 65862015
Hyphenated Format 65862-015

Supplemental Identifiers

RxCUI
308192 308194
UPC
0365862015013
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 ANDA065256 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 875 mg/1
source: ndc
Packaging
  • 100 TABLET, FILM COATED in 1 BOTTLE (65862-015-01)
  • 500 TABLET, FILM COATED in 1 BOTTLE (65862-015-05)
  • 20 TABLET, FILM COATED in 1 BOTTLE (65862-015-20)
source: ndc

Packages (3)

65862-015-01 100 TABLET, FILM COATED in 1 BOTTLE (65862-015-01) 65862-015-05 500 TABLET, FILM COATED in 1 BOTTLE (65862-015-05) 65862-015-20 20 TABLET, FILM COATED in 1 BOTTLE (65862-015-20)

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": "ee0e12cd-e881-4048-a0fb-74bd771cb9aa", "openfda": {"upc": ["0365862015013"], "unii": ["804826J2HU"], "rxcui": ["308192", "308194"], "spl_set_id": ["99103779-6d2f-4e4b-9b7f-0b24d7c6bf4e"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (65862-015-01)", "package_ndc": "65862-015-01", "marketing_start_date": "20051109"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (65862-015-05)", "package_ndc": "65862-015-05", "marketing_start_date": "20051109"}, {"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE (65862-015-20)", "package_ndc": "65862-015-20", "marketing_start_date": "20051109"}], "brand_name": "Amoxicillin", "product_id": "65862-015_ee0e12cd-e881-4048-a0fb-74bd771cb9aa", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Penicillin-class Antibacterial [EPC]", "Penicillins [CS]"], "product_ndc": "65862-015", "generic_name": "Amoxicillin", "labeler_name": "Aurobindo Pharma Limited", "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"}