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 POWDER, FOR SUSPENSION
Routes
ORAL
Active Ingredients

amoxicillin 250 mg/5mL

Manufacturer
Preferred Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 68788-8759
Product ID 68788-8759_4c858be1-f077-4602-b424-bf8b8c7d4da4
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA065322
Listing Expiration 2027-12-31
Marketing Start 2024-10-17

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 687888759
Hyphenated Format 68788-8759

Supplemental Identifiers

RxCUI
239191
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 ANDA065322 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 250 mg/5mL
source: ndc
Packaging
  • 150 mL in 1 BOTTLE (68788-8759-1)
source: ndc

Packages (1)

68788-8759-1 150 mL in 1 BOTTLE (68788-8759-1)

Ingredients (1)

amoxicillin (250 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": "4c858be1-f077-4602-b424-bf8b8c7d4da4", "openfda": {"unii": ["804826J2HU"], "rxcui": ["239191"], "spl_set_id": ["0ce05282-995c-461e-b807-facb1fcbb405"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "150 mL in 1 BOTTLE (68788-8759-1)", "package_ndc": "68788-8759-1", "marketing_start_date": "20241017"}], "brand_name": "Amoxicillin", "product_id": "68788-8759_4c858be1-f077-4602-b424-bf8b8c7d4da4", "dosage_form": "POWDER, FOR SUSPENSION", "pharm_class": ["Penicillin-class Antibacterial [EPC]", "Penicillins [CS]"], "product_ndc": "68788-8759", "generic_name": "Amoxicillin", "labeler_name": "Preferred Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amoxicillin", "active_ingredients": [{"name": "AMOXICILLIN", "strength": "250 mg/5mL"}], "application_number": "ANDA065322", "marketing_category": "ANDA", "marketing_start_date": "20241017", "listing_expiration_date": "20271231"}