amoxicillin 500 mg
Generic: amoxicillin
Labeler: health department, oklahoma stateDrug Facts
Product Profile
Brand Name
amoxicillin 500 mg
Generic Name
amoxicillin
Labeler
health department, oklahoma state
Dosage Form
CAPSULE
Routes
Active Ingredients
amoxicillin 500 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
83112-500
Product ID
83112-500_45d711af-0b7c-998e-e063-6294a90a5ea4
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA065271
Listing Expiration
2026-12-31
Marketing Start
2005-11-09
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
83112500
Hyphenated Format
83112-500
Supplemental Identifiers
RxCUI
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 500 mg (source: ndc)
Generic Name
amoxicillin (source: ndc)
Application Number
ANDA065271 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 500 mg/1
Packaging
- 21 CAPSULE in 1 BLISTER PACK (83112-500-21)
- 30 CAPSULE in 1 BLISTER PACK (83112-500-30)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "45d711af-0b7c-998e-e063-6294a90a5ea4", "openfda": {"unii": ["804826J2HU"], "rxcui": ["308191"], "spl_set_id": ["f049551b-4708-eb13-e053-2a95a90afd1f"], "manufacturer_name": ["Health Department, Oklahoma State"]}, "finished": true, "packaging": [{"sample": false, "description": "21 CAPSULE in 1 BLISTER PACK (83112-500-21)", "package_ndc": "83112-500-21", "marketing_start_date": "20051109"}, {"sample": false, "description": "30 CAPSULE in 1 BLISTER PACK (83112-500-30)", "package_ndc": "83112-500-30", "marketing_start_date": "20051109"}], "brand_name": "Amoxicillin 500 mg", "product_id": "83112-500_45d711af-0b7c-998e-e063-6294a90a5ea4", "dosage_form": "CAPSULE", "pharm_class": ["Penicillin-class Antibacterial [EPC]", "Penicillins [CS]"], "product_ndc": "83112-500", "generic_name": "Amoxicillin", "labeler_name": "Health Department, Oklahoma State", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amoxicillin 500 mg", "active_ingredients": [{"name": "AMOXICILLIN", "strength": "500 mg/1"}], "application_number": "ANDA065271", "marketing_category": "ANDA", "marketing_start_date": "20051109", "listing_expiration_date": "20261231"}