amoxicillin

Generic: amoxicillin

Labeler: sandoz inc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name amoxicillin
Generic Name amoxicillin
Labeler sandoz inc
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

amoxicillin 875 mg/1

Manufacturer
Sandoz Inc

Identifiers & Regulatory

Product NDC 0781-5061
Product ID 0781-5061_6aa02079-d11c-4d2f-acaf-9548dd9a7ed6
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA065228
Listing Expiration 2026-12-31
Marketing Start 2005-07-13

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 07815061
Hyphenated Format 0781-5061

Supplemental Identifiers

RxCUI
239191 308182 308189 308191 308192 308194 313797 313850
UPC
0307816156526 0307812020012 0307816041587 0307815060015 0307815061012 0307816157523 0307816039584 0307812613016
UNII
804826J2HU

Packaging Origin

Original Packager
true

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 ANDA065228 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 875 mg/1
source: ndc
Packaging
  • 100 TABLET, FILM COATED in 1 BOTTLE (0781-5061-01)
  • 20 TABLET, FILM COATED in 1 BOTTLE (0781-5061-20)
source: ndc

Packages (2)

0781-5061-01 100 TABLET, FILM COATED in 1 BOTTLE (0781-5061-01) 0781-5061-20 20 TABLET, FILM COATED in 1 BOTTLE (0781-5061-20)

Ingredients (1)

amoxicillin (875 mg/1)

Linked Drug Pages (1)

Amoxicillin ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "6aa02079-d11c-4d2f-acaf-9548dd9a7ed6", "openfda": {"upc": ["0307816156526", "0307812020012", "0307816041587", "0307815060015", "0307815061012", "0307816157523", "0307816039584", "0307812613016"], "unii": ["804826J2HU"], "rxcui": ["239191", "308182", "308189", "308191", "308192", "308194", "313797", "313850"], "spl_set_id": ["13bd4214-9b7f-425b-af5f-fc1ddc678230"], "manufacturer_name": ["Sandoz Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (0781-5061-01)", "package_ndc": "0781-5061-01", "marketing_start_date": "20050713"}, {"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE (0781-5061-20)", "package_ndc": "0781-5061-20", "marketing_start_date": "20050713"}], "brand_name": "Amoxicillin", "product_id": "0781-5061_6aa02079-d11c-4d2f-acaf-9548dd9a7ed6", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Penicillin-class Antibacterial [EPC]", "Penicillins [CS]"], "product_ndc": "0781-5061", "generic_name": "Amoxicillin", "labeler_name": "Sandoz Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amoxicillin", "active_ingredients": [{"name": "AMOXICILLIN", "strength": "875 mg/1"}], "application_number": "ANDA065228", "marketing_category": "ANDA", "marketing_start_date": "20050713", "listing_expiration_date": "20261231"}