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 POWDER, FOR SUSPENSION
Routes
ORAL
Active Ingredients

amoxicillin 125 mg/5mL

Manufacturer
Aurobindo Pharma Limited

Identifiers & Regulatory

Product NDC 65862-706
Product ID 65862-706_f4a410c9-3a78-48f9-8195-915896a974ff
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 65862706
Hyphenated Format 65862-706

Supplemental Identifiers

RxCUI
239191 313797
UPC
0365862707017 0365862706010
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 ANDA204030 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 125 mg/5mL
source: ndc
Packaging
  • 100 mL in 1 BOTTLE (65862-706-01)
  • 150 mL in 1 BOTTLE (65862-706-55)
  • 80 mL in 1 BOTTLE (65862-706-80)
source: ndc

Packages (3)

65862-706-01 100 mL in 1 BOTTLE (65862-706-01) 65862-706-55 150 mL in 1 BOTTLE (65862-706-55) 65862-706-80 80 mL in 1 BOTTLE (65862-706-80)

Ingredients (1)

amoxicillin (125 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": "f4a410c9-3a78-48f9-8195-915896a974ff", "openfda": {"upc": ["0365862707017", "0365862706010"], "unii": ["804826J2HU"], "rxcui": ["239191", "313797"], "spl_set_id": ["234d0dfc-cb24-413f-b798-129c73eb848e"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 mL in 1 BOTTLE (65862-706-01)", "package_ndc": "65862-706-01", "marketing_start_date": "20140915"}, {"sample": false, "description": "150 mL in 1 BOTTLE (65862-706-55)", "package_ndc": "65862-706-55", "marketing_start_date": "20140915"}, {"sample": false, "description": "80 mL in 1 BOTTLE (65862-706-80)", "package_ndc": "65862-706-80", "marketing_start_date": "20140915"}], "brand_name": "Amoxicillin", "product_id": "65862-706_f4a410c9-3a78-48f9-8195-915896a974ff", "dosage_form": "POWDER, FOR SUSPENSION", "pharm_class": ["Penicillin-class Antibacterial [EPC]", "Penicillins [CS]"], "product_ndc": "65862-706", "generic_name": "Amoxicillin", "labeler_name": "Aurobindo Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amoxicillin", "active_ingredients": [{"name": "AMOXICILLIN", "strength": "125 mg/5mL"}], "application_number": "ANDA204030", "marketing_category": "ANDA", "marketing_start_date": "20140915", "listing_expiration_date": "20261231"}