amoxicillin and clavulanate potassium

Generic: amoxicillin and clavulanate potassium

Labeler: cambridge therapeutics technologies, llc
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 cambridge therapeutics technologies, llc
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

amoxicillin 250 mg/1, clavulanate potassium 125 mg/1

Manufacturer
Cambridge Therapeutics Technologies, LLC

Identifiers & Regulatory

Product NDC 70882-111
Product ID 70882-111_f0063b1e-af9e-474d-96b9-0b3aa1a37ea2
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA065189
Listing Expiration 2026-12-31
Marketing Start 2005-08-23

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 70882111
Hyphenated Format 70882-111

Supplemental Identifiers

RxCUI
562251
UPC
0370882111201
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 ANDA065189 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 250 mg/1
  • 125 mg/1
source: ndc
Packaging
  • 20 TABLET, FILM COATED in 1 BLISTER PACK (70882-111-20)
source: ndc

Packages (1)

70882-111-20 20 TABLET, FILM COATED in 1 BLISTER PACK (70882-111-20)

Ingredients (2)

amoxicillin (250 mg/1) clavulanate potassium (125 mg/1)

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": "f0063b1e-af9e-474d-96b9-0b3aa1a37ea2", "openfda": {"upc": ["0370882111201"], "unii": ["804826J2HU", "Q42OMW3AT8"], "rxcui": ["562251"], "spl_set_id": ["a4c9694c-f539-470e-bfe3-8723fa1c343d"], "manufacturer_name": ["Cambridge Therapeutics Technologies, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET, FILM COATED in 1 BLISTER PACK (70882-111-20)", "package_ndc": "70882-111-20", "marketing_start_date": "20050823"}], "brand_name": "Amoxicillin and Clavulanate Potassium", "product_id": "70882-111_f0063b1e-af9e-474d-96b9-0b3aa1a37ea2", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Penicillin-class Antibacterial [EPC]", "Penicillins [CS]", "beta Lactamase Inhibitor [EPC]", "beta Lactamase Inhibitors [MoA]"], "product_ndc": "70882-111", "generic_name": "Amoxicillin and Clavulanate Potassium", "labeler_name": "Cambridge Therapeutics Technologies, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amoxicillin and Clavulanate Potassium", "active_ingredients": [{"name": "AMOXICILLIN", "strength": "250 mg/1"}, {"name": "CLAVULANATE POTASSIUM", "strength": "125 mg/1"}], "application_number": "ANDA065189", "marketing_category": "ANDA", "marketing_start_date": "20050823", "listing_expiration_date": "20261231"}