amoxicillin and clavulanate potassium

Generic: amoxicillin and clavulanate potassium

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

Drug Facts

Product Profile

Brand Name amoxicillin and clavulanate potassium
Generic Name amoxicillin and clavulanate potassium
Labeler preferred pharmaceuticals, inc.
Dosage Form POWDER, FOR SUSPENSION
Routes
ORAL
Active Ingredients

amoxicillin 600 mg/5mL, clavulanate potassium 42.9 mg/5mL

Manufacturer
Preferred Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 68788-0483
Product ID 68788-0483_e51cf486-cd20-464d-a9e5-917ee699ad43
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA201091
Listing Expiration 2027-12-31
Marketing Start 2011-11-07

Pharmacologic Class

Classes
penicillin-class antibacterial [epc] penicillins [cs] beta lactamase inhibitor [epc] beta lactamase inhibitors [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 687880483
Hyphenated Format 68788-0483

Supplemental Identifiers

RxCUI
617993
UNII
804826J2HU Q42OMW3AT8

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 and clavulanate potassium (source: ndc)
Generic Name amoxicillin and clavulanate potassium (source: ndc)
Application Number ANDA201091 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 600 mg/5mL
  • 42.9 mg/5mL
source: ndc
Packaging
  • 125 mL in 1 BOTTLE (68788-0483-1)
  • 75 mL in 1 BOTTLE (68788-0483-7)
source: ndc

Packages (2)

68788-0483-1 125 mL in 1 BOTTLE (68788-0483-1) 68788-0483-7 75 mL in 1 BOTTLE (68788-0483-7)

Ingredients (2)

amoxicillin (600 mg/5mL) clavulanate potassium (42.9 mg/5mL)

Linked Drug Pages (1)

Amoxicillin and Clavulanate Potassium ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "e51cf486-cd20-464d-a9e5-917ee699ad43", "openfda": {"unii": ["804826J2HU", "Q42OMW3AT8"], "rxcui": ["617993"], "spl_set_id": ["22a387bd-92ce-4ebc-b475-20d7750a2507"], "manufacturer_name": ["Preferred Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "125 mL in 1 BOTTLE (68788-0483-1)", "package_ndc": "68788-0483-1", "marketing_start_date": "20111107"}, {"sample": false, "description": "75 mL in 1 BOTTLE (68788-0483-7)", "package_ndc": "68788-0483-7", "marketing_start_date": "20111107"}], "brand_name": "Amoxicillin and Clavulanate Potassium", "product_id": "68788-0483_e51cf486-cd20-464d-a9e5-917ee699ad43", "dosage_form": "POWDER, FOR SUSPENSION", "pharm_class": ["Penicillin-class Antibacterial [EPC]", "Penicillins [CS]", "beta Lactamase Inhibitor [EPC]", "beta Lactamase Inhibitors [MoA]"], "product_ndc": "68788-0483", "generic_name": "Amoxicillin and Clavulanate Potassium", "labeler_name": "Preferred Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amoxicillin and Clavulanate Potassium", "active_ingredients": [{"name": "AMOXICILLIN", "strength": "600 mg/5mL"}, {"name": "CLAVULANATE POTASSIUM", "strength": "42.9 mg/5mL"}], "application_number": "ANDA201091", "marketing_category": "ANDA", "marketing_start_date": "20111107", "listing_expiration_date": "20271231"}