amoxicillin and clavulanate potassium

Generic: amoxicillin and clavulanate potassium

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

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

Manufacturer
NuCare Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 68071-3807
Product ID 68071-3807_30144cfc-0fb1-8d62-e063-6394a90acba4
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA201090
Listing Expiration 2026-12-31
Marketing Start 2011-12-20

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 680713807
Hyphenated Format 68071-3807

Supplemental Identifiers

RxCUI
617423
UPC
0368071380712
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 ANDA201090 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 200 mg/5mL
  • 28.5 mg/5mL
source: ndc
Packaging
  • 100 mL in 1 BOTTLE (68071-3807-1)
source: ndc

Packages (1)

68071-3807-1 100 mL in 1 BOTTLE (68071-3807-1)

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": "30144cfc-0fb1-8d62-e063-6394a90acba4", "openfda": {"upc": ["0368071380712"], "unii": ["804826J2HU", "Q42OMW3AT8"], "rxcui": ["617423"], "spl_set_id": ["30144e2e-d336-8fa3-e063-6394a90a6068"], "manufacturer_name": ["NuCare Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 mL in 1 BOTTLE (68071-3807-1)", "package_ndc": "68071-3807-1", "marketing_start_date": "20250311"}], "brand_name": "Amoxicillin and Clavulanate Potassium", "product_id": "68071-3807_30144cfc-0fb1-8d62-e063-6394a90acba4", "dosage_form": "POWDER, FOR SUSPENSION", "pharm_class": ["Penicillin-class Antibacterial [EPC]", "Penicillins [CS]", "beta Lactamase Inhibitor [EPC]", "beta Lactamase Inhibitors [MoA]"], "product_ndc": "68071-3807", "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": "200 mg/5mL"}, {"name": "CLAVULANATE POTASSIUM", "strength": "28.5 mg/5mL"}], "application_number": "ANDA201090", "marketing_category": "ANDA", "marketing_start_date": "20111220", "listing_expiration_date": "20261231"}