amoxicillin and clavulanate potassium

Generic: amoxicillin and clavulanate potassium

Labeler: teva pharmaceuticals usa, 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 teva pharmaceuticals usa, inc.
Dosage Form POWDER, FOR SUSPENSION
Routes
ORAL
Active Ingredients

amoxicillin 200 mg/5mL, clavulanate potassium 28.5 mg/5mL

Manufacturer
Teva Pharmaceuticals USA, Inc.

Identifiers & Regulatory

Product NDC 0093-2277
Product ID 0093-2277_aaf9ce2f-41c3-489c-b5c1-f4f553d84854
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA065089
Listing Expiration 2026-12-31
Marketing Start 2005-01-13

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 00932277
Hyphenated Format 0093-2277

Supplemental Identifiers

RxCUI
562508 617296 617423 617430
UPC
0300932274341 0300932275348
UNII
Q42OMW3AT8 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 and clavulanate potassium (source: ndc)
Generic Name amoxicillin and clavulanate potassium (source: ndc)
Application Number ANDA065089 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 200 mg/5mL
  • 28.5 mg/5mL
source: ndc
Packaging
  • 100 mL in 1 BOTTLE (0093-2277-73)
source: ndc

Packages (1)

0093-2277-73 100 mL in 1 BOTTLE (0093-2277-73)

Ingredients (2)

amoxicillin (200 mg/5mL) clavulanate potassium (28.5 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": "aaf9ce2f-41c3-489c-b5c1-f4f553d84854", "openfda": {"upc": ["0300932274341", "0300932275348"], "unii": ["Q42OMW3AT8", "804826J2HU"], "rxcui": ["562508", "617296", "617423", "617430"], "spl_set_id": ["963e7bea-ff5d-420a-9cb2-e4aefb534b33"], "manufacturer_name": ["Teva Pharmaceuticals USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 mL in 1 BOTTLE (0093-2277-73)", "package_ndc": "0093-2277-73", "marketing_start_date": "20050113"}], "brand_name": "Amoxicillin and Clavulanate Potassium", "product_id": "0093-2277_aaf9ce2f-41c3-489c-b5c1-f4f553d84854", "dosage_form": "POWDER, FOR SUSPENSION", "pharm_class": ["Penicillin-class Antibacterial [EPC]", "Penicillins [CS]", "beta Lactamase Inhibitor [EPC]", "beta Lactamase Inhibitors [MoA]"], "product_ndc": "0093-2277", "generic_name": "Amoxicillin and Clavulanate Potassium", "labeler_name": "Teva Pharmaceuticals USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amoxicillin and Clavulanate Potassium", "active_ingredients": [{"name": "AMOXICILLIN", "strength": "200 mg/5mL"}, {"name": "CLAVULANATE POTASSIUM", "strength": "28.5 mg/5mL"}], "application_number": "ANDA065089", "marketing_category": "ANDA", "marketing_start_date": "20050113", "listing_expiration_date": "20261231"}