Package 82982-022-20

Brand: amoxicillin

Generic: amoxicillin
NDC Package

Package Facts

Identity

Package NDC 82982-022-20
Digits Only 8298202220
Product NDC 82982-022
Product ID 82982-022_198cdc87-f7b3-0a31-e063-6394a90a7e77
Description

20 CAPSULE in 1 BOTTLE (82982-022-20)

Marketing

Marketing Status
Discontinued 2026-06-30
Brand amoxicillin
Generic amoxicillin
Sample Package No

Linked Drug Pages (1)

Amoxicillin ndc-match (0.95)

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"}