amoxicillin and clavulanate potassium

Generic: amoxicillin and clavulanate potassium

Labeler: proficient rx lp
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 proficient rx lp
Dosage Form SUSPENSION
Routes
ORAL
Active Ingredients

amoxicillin 600 mg/5mL, clavulanate potassium 42.9 mg/5mL

Manufacturer
Proficient Rx LP

Identifiers & Regulatory

Product NDC 71205-620
Product ID 71205-620_6852b72b-bec8-43c3-a1c3-1fea0c6b633f
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA065358
Listing Expiration 2026-12-31
Marketing Start 2007-08-13

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 71205620
Hyphenated Format 71205-620

Supplemental Identifiers

RxCUI
617993
UPC
0371205620752
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 ANDA065358 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 600 mg/5mL
  • 42.9 mg/5mL
source: ndc
Packaging
  • 75 mL in 1 BOTTLE, DISPENSING (71205-620-75)
source: ndc

Packages (1)

Ingredients (2)

amoxicillin (600 mg/5mL) clavulanate potassium (42.9 mg/5mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "6852b72b-bec8-43c3-a1c3-1fea0c6b633f", "openfda": {"upc": ["0371205620752"], "unii": ["804826J2HU", "Q42OMW3AT8"], "rxcui": ["617993"], "spl_set_id": ["474c822b-dc3d-4a55-8159-2b4b799d535b"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "75 mL in 1 BOTTLE, DISPENSING (71205-620-75)", "package_ndc": "71205-620-75", "marketing_start_date": "20211101"}], "brand_name": "Amoxicillin and Clavulanate Potassium", "product_id": "71205-620_6852b72b-bec8-43c3-a1c3-1fea0c6b633f", "dosage_form": "SUSPENSION", "pharm_class": ["Penicillin-class Antibacterial [EPC]", "Penicillins [CS]", "beta Lactamase Inhibitor [EPC]", "beta Lactamase Inhibitors [MoA]"], "product_ndc": "71205-620", "generic_name": "Amoxicillin and Clavulanate Potassium", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amoxicillin and Clavulanate Potassium", "active_ingredients": [{"name": "AMOXICILLIN", "strength": "600 mg/5mL"}, {"name": "CLAVULANATE POTASSIUM", "strength": "42.9 mg/5mL"}], "application_number": "ANDA065358", "marketing_category": "ANDA", "marketing_start_date": "20070813", "listing_expiration_date": "20261231"}