amoxicillin and clavulanate potassium
Generic: amoxicillin and clavulanate potassium
Labeler: nucare pharmaceuticals,inc.Drug Facts
Product Profile
Brand Name
amoxicillin and clavulanate potassium
Generic Name
amoxicillin and clavulanate potassium
Labeler
nucare pharmaceuticals,inc.
Dosage Form
TABLET
Routes
Active Ingredients
amoxicillin 875 mg/1, clavulanate potassium 125 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
68071-5026
Product ID
68071-5026_4098273b-4560-4119-e063-6294a90a3a1f
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA203824
Listing Expiration
2026-12-31
Marketing Start
2016-08-23
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
680715026
Hyphenated Format
68071-5026
Supplemental Identifiers
RxCUI
UPC
UNII
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
ANDA203824 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 875 mg/1
- 125 mg/1
Packaging
- 14 TABLET in 1 BOTTLE (68071-5026-4)
Packages (1)
Ingredients (2)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4098273b-4560-4119-e063-6294a90a3a1f", "openfda": {"upc": ["0368071502640"], "unii": ["804826J2HU", "Q42OMW3AT8"], "rxcui": ["562508"], "spl_set_id": ["9015d3dc-1ab4-2582-e053-2995a90a1679"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "14 TABLET in 1 BOTTLE (68071-5026-4)", "package_ndc": "68071-5026-4", "marketing_start_date": "20190814"}], "brand_name": "Amoxicillin and Clavulanate Potassium", "product_id": "68071-5026_4098273b-4560-4119-e063-6294a90a3a1f", "dosage_form": "TABLET", "pharm_class": ["Penicillin-class Antibacterial [EPC]", "Penicillins [CS]", "beta Lactamase Inhibitor [EPC]", "beta Lactamase Inhibitors [MoA]"], "product_ndc": "68071-5026", "generic_name": "Amoxicillin and Clavulanate Potassium", "labeler_name": "NuCare Pharmaceuticals,Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amoxicillin and Clavulanate Potassium", "active_ingredients": [{"name": "AMOXICILLIN", "strength": "875 mg/1"}, {"name": "CLAVULANATE POTASSIUM", "strength": "125 mg/1"}], "application_number": "ANDA203824", "marketing_category": "ANDA", "marketing_start_date": "20160823", "listing_expiration_date": "20261231"}