amoxicillin and clavulanate potassium (71335-2999)

Drug Facts

Product Profile

Brand Name amoxicillin and clavulanate potassium

Generic Name amoxicillin and clavulanate potassium

Labeler bryant ranch prepack

Dosage Form TABLET, FILM COATED

Routes

ORAL

Active Ingredients

amoxicillin 500 mg/1, clavulanate potassium 125 mg/1

Manufacturer

Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 71335-2999

Product ID 71335-2999_6e01dd3f-c563-4091-a07f-52bbb6d51b0a

Product Type HUMAN PRESCRIPTION DRUG

Marketing Category ANDA

Application Number ANDA065064

Listing Expiration 2026-12-31

Marketing Start 2002-03-15

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 713352999

Hyphenated Format 71335-2999

Supplemental Identifiers

RxCUI

617296

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 ANDA065064 (source: ndc)

Routes

ORAL

source: ndc

Resolved Composition

Strengths

500 mg/1
125 mg/1

source: ndc

Packaging

20 TABLET, FILM COATED in 1 BOTTLE (71335-2999-1)

source: ndc

Packages (1)

71335-2999-1 20 TABLET, FILM COATED in 1 BOTTLE (71335-2999-1)

Ingredients (2)

amoxicillin (500 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": "6e01dd3f-c563-4091-a07f-52bbb6d51b0a", "openfda": {"unii": ["804826J2HU", "Q42OMW3AT8"], "rxcui": ["617296"], "spl_set_id": ["22cd4e96-2288-470c-9264-8058cd7db9b0"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE (71335-2999-1)", "package_ndc": "71335-2999-1", "marketing_start_date": "20251105"}], "brand_name": "Amoxicillin and Clavulanate Potassium", "product_id": "71335-2999_6e01dd3f-c563-4091-a07f-52bbb6d51b0a", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Penicillin-class Antibacterial [EPC]", "Penicillins [CS]", "beta Lactamase Inhibitor [EPC]", "beta Lactamase Inhibitors [MoA]"], "product_ndc": "71335-2999", "generic_name": "Amoxicillin and Clavulanate Potassium", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amoxicillin and Clavulanate Potassium", "active_ingredients": [{"name": "AMOXICILLIN", "strength": "500 mg/1"}, {"name": "CLAVULANATE POTASSIUM", "strength": "125 mg/1"}], "application_number": "ANDA065064", "marketing_category": "ANDA", "marketing_start_date": "20020315", "listing_expiration_date": "20261231"}