amoxicillin and clavulanate potassium
Generic: amoxicillin and clavulanate potassium
Labeler: proficient rx lpDrug Facts
Product Profile
Brand Name
amoxicillin and clavulanate potassium
Generic Name
amoxicillin and clavulanate potassium
Labeler
proficient rx lp
Dosage Form
SUSPENSION
Routes
Active Ingredients
amoxicillin 600 mg/5mL, clavulanate potassium 42.9 mg/5mL
Manufacturer
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
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
71205620
Hyphenated Format
71205-620
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
ANDA065358 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 600 mg/5mL
- 42.9 mg/5mL
Packaging
- 75 mL in 1 BOTTLE, DISPENSING (71205-620-75)
Packages (1)
Ingredients (2)
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"}