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 CAPSULE
Routes
ORAL
Active Ingredients

amoxicillin 500 mg/1

Manufacturer
Aurobindo Pharma Limited

Identifiers & Regulatory

Product NDC 65862-017
Product ID 65862-017_4dc94f3c-990d-476f-a88e-df9967570eec
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA065271
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 65862017
Hyphenated Format 65862-017

Supplemental Identifiers

RxCUI
308182 308191
UPC
0365862017208 0365862016201
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 ANDA065271 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 500 mg/1
source: ndc
Packaging
  • 100 CAPSULE in 1 BOTTLE (65862-017-01)
  • 500 CAPSULE in 1 BOTTLE (65862-017-05)
  • 20 CAPSULE in 1 BOTTLE (65862-017-20)
  • 30 CAPSULE in 1 BOTTLE (65862-017-30)
  • 50 CAPSULE in 1 BOTTLE (65862-017-50)
source: ndc

Packages (5)

Ingredients (1)

amoxicillin (500 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4dc94f3c-990d-476f-a88e-df9967570eec", "openfda": {"upc": ["0365862017208", "0365862016201"], "unii": ["804826J2HU"], "rxcui": ["308182", "308191"], "spl_set_id": ["7e3a4517-1934-4e03-b96b-4ad65ab076c5"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (65862-017-01)", "package_ndc": "65862-017-01", "marketing_start_date": "20051109"}, {"sample": false, "description": "500 CAPSULE in 1 BOTTLE (65862-017-05)", "package_ndc": "65862-017-05", "marketing_start_date": "20051109"}, {"sample": false, "description": "20 CAPSULE in 1 BOTTLE (65862-017-20)", "package_ndc": "65862-017-20", "marketing_start_date": "20051109"}, {"sample": false, "description": "30 CAPSULE in 1 BOTTLE (65862-017-30)", "package_ndc": "65862-017-30", "marketing_start_date": "20051109"}, {"sample": false, "description": "50 CAPSULE in 1 BOTTLE (65862-017-50)", "package_ndc": "65862-017-50", "marketing_start_date": "20051109"}], "brand_name": "Amoxicillin", "product_id": "65862-017_4dc94f3c-990d-476f-a88e-df9967570eec", "dosage_form": "CAPSULE", "pharm_class": ["Penicillin-class Antibacterial [EPC]", "Penicillins [CS]"], "product_ndc": "65862-017", "generic_name": "Amoxicillin", "labeler_name": "Aurobindo Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amoxicillin", "active_ingredients": [{"name": "AMOXICILLIN", "strength": "500 mg/1"}], "application_number": "ANDA065271", "marketing_category": "ANDA", "marketing_start_date": "20051109", "listing_expiration_date": "20261231"}