amoxicillin

Generic: amoxicillin

Labeler: preferred pharmaceuticals inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

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

amoxicillin 875 mg/1

Manufacturer
Preferred Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 68788-4062
Product ID 68788-4062_6a3f7e6c-fec2-41da-a070-00a02e64c920
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA065255
Listing Expiration 2027-12-31
Marketing Start 2026-01-28

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 687884062
Hyphenated Format 68788-4062

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 ANDA065255 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 875 mg/1
source: ndc
Packaging
  • 20 TABLET, COATED in 1 BOTTLE (68788-4062-2)
source: ndc

Packages (1)

68788-4062-2 20 TABLET, COATED in 1 BOTTLE (68788-4062-2)

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": "6a3f7e6c-fec2-41da-a070-00a02e64c920", "openfda": {"unii": ["804826J2HU"], "rxcui": ["308194"], "spl_set_id": ["6a3f7e6c-fec2-41da-a070-00a02e64c920"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET, COATED in 1 BOTTLE (68788-4062-2)", "package_ndc": "68788-4062-2", "marketing_start_date": "20260128"}], "brand_name": "Amoxicillin", "product_id": "68788-4062_6a3f7e6c-fec2-41da-a070-00a02e64c920", "dosage_form": "TABLET, COATED", "pharm_class": ["Penicillin-class Antibacterial [EPC]", "Penicillins [CS]"], "product_ndc": "68788-4062", "generic_name": "Amoxicillin", "labeler_name": "Preferred Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amoxicillin", "active_ingredients": [{"name": "AMOXICILLIN", "strength": "875 mg/1"}], "application_number": "ANDA065255", "marketing_category": "ANDA", "marketing_start_date": "20260128", "listing_expiration_date": "20271231"}