amoxicillin and clavulanate potassium

Generic: amoxicillin and clavulanate potassium

Labeler: northstar rxllc
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 northstar rxllc
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

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

Manufacturer
Northstar RxLLC

Identifiers & Regulatory

Product NDC 16714-476
Product ID 16714-476_3327c23e-bb50-425b-989d-eea2568c99f6
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA065189
Marketing Start 2015-11-01
Marketing End 2026-06-30

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 16714476
Hyphenated Format 16714-476

Supplemental Identifiers

RxCUI
562251 562508 617296
UPC
0316714477015 0316714014012 0316714476018
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 ANDA065189 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 250 mg/1
  • 125 mg/1
source: ndc
Packaging
  • 30 TABLET, FILM COATED in 1 BOTTLE (16714-476-01)
source: ndc

Packages (1)

16714-476-01 30 TABLET, FILM COATED in 1 BOTTLE (16714-476-01)

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": "3327c23e-bb50-425b-989d-eea2568c99f6", "openfda": {"upc": ["0316714477015", "0316714014012", "0316714476018"], "unii": ["Q42OMW3AT8", "804826J2HU"], "rxcui": ["562251", "562508", "617296"], "spl_set_id": ["d6bff811-a6ea-4e4e-a4eb-b34b966cdb40"], "manufacturer_name": ["Northstar RxLLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (16714-476-01)", "package_ndc": "16714-476-01", "marketing_end_date": "20260630", "marketing_start_date": "20151101"}], "brand_name": "Amoxicillin and Clavulanate Potassium", "product_id": "16714-476_3327c23e-bb50-425b-989d-eea2568c99f6", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Penicillin-class Antibacterial [EPC]", "Penicillins [CS]", "beta Lactamase Inhibitor [EPC]", "beta Lactamase Inhibitors [MoA]"], "product_ndc": "16714-476", "generic_name": "Amoxicillin and Clavulanate Potassium", "labeler_name": "Northstar RxLLC", "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_end_date": "20260630", "marketing_start_date": "20151101"}