amoxicillin

Generic: amoxicillin

Labeler: pharmasource meds, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name amoxicillin
Generic Name amoxicillin
Labeler pharmasource meds, llc
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

amoxicillin 500 mg/1

Manufacturer
Pharmasource Meds, LLC

Identifiers & Regulatory

Product NDC 82982-022
Product ID 82982-022_198cdc87-f7b3-0a31-e063-6394a90a7e77
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA065271
Marketing Start 2023-02-17
Marketing End 2026-06-30

Pharmacologic Class

Classes
penicillin-class antibacterial [epc] penicillins [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 82982022
Hyphenated Format 82982-022

Supplemental Identifiers

RxCUI
308191
UPC
0382982022202
UNII
804826J2HU

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 (source: ndc)
Generic Name amoxicillin (source: ndc)
Application Number ANDA065271 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 500 mg/1
source: ndc
Packaging
  • 20 CAPSULE in 1 BOTTLE (82982-022-20)
source: ndc

Packages (1)

Ingredients (1)

amoxicillin (500 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "198cdc87-f7b3-0a31-e063-6394a90a7e77", "openfda": {"upc": ["0382982022202"], "unii": ["804826J2HU"], "rxcui": ["308191"], "spl_set_id": ["f4e99b4f-2cf4-ba35-e053-2a95a90ada5f"], "manufacturer_name": ["Pharmasource Meds, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "20 CAPSULE in 1 BOTTLE (82982-022-20)", "package_ndc": "82982-022-20", "marketing_end_date": "20260630", "marketing_start_date": "20230217"}], "brand_name": "Amoxicillin", "product_id": "82982-022_198cdc87-f7b3-0a31-e063-6394a90a7e77", "dosage_form": "CAPSULE", "pharm_class": ["Penicillin-class Antibacterial [EPC]", "Penicillins [CS]"], "product_ndc": "82982-022", "generic_name": "Amoxicillin", "labeler_name": "Pharmasource Meds, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amoxicillin", "active_ingredients": [{"name": "AMOXICILLIN", "strength": "500 mg/1"}], "application_number": "ANDA065271", "marketing_category": "ANDA", "marketing_end_date": "20260630", "marketing_start_date": "20230217"}