Package 76420-138-20

Brand: amoxicillin

Generic: amoxicillin
NDC Package

Package Facts

Identity

Package NDC 76420-138-20
Digits Only 7642013820
Product NDC 76420-138
Description

20 TABLET, COATED in 1 BOTTLE (76420-138-20)

Marketing

Marketing Status
Marketed Since 2022-03-04
Brand amoxicillin
Generic amoxicillin
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "d964632f-4590-9500-e053-2995a90a992d", "openfda": {"unii": ["804826J2HU"], "rxcui": ["308194"], "spl_set_id": ["23b7a1fe-4e23-44ec-bc51-5209427c88ce"], "manufacturer_name": ["Asclemed USA, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET, COATED in 1 BOTTLE (76420-138-20)", "package_ndc": "76420-138-20", "marketing_start_date": "20220304"}], "brand_name": "Amoxicillin", "product_id": "76420-138_d964632f-4590-9500-e053-2995a90a992d", "dosage_form": "TABLET, COATED", "pharm_class": ["Penicillin-class Antibacterial [EPC]", "Penicillins [CS]"], "product_ndc": "76420-138", "generic_name": "Amoxicillin", "labeler_name": "Asclemed USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amoxicillin", "active_ingredients": [{"name": "AMOXICILLIN", "strength": "875 mg/1"}], "application_number": "ANDA065255", "marketing_category": "ANDA", "marketing_start_date": "20060329", "listing_expiration_date": "20261231"}