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 POWDER, FOR SUSPENSION
Routes
ORAL
Active Ingredients

amoxicillin 200 mg/5mL

Manufacturer
Sandoz Inc

Identifiers & Regulatory

Product NDC 0781-6156
Product ID 0781-6156_6aa02079-d11c-4d2f-acaf-9548dd9a7ed6
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA065378
Listing Expiration 2026-12-31
Marketing Start 2007-03-26

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 07816156
Hyphenated Format 0781-6156

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 ANDA065378 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 200 mg/5mL
source: ndc
Packaging
  • 100 mL in 1 BOTTLE (0781-6156-46)
  • 50 mL in 1 BOTTLE (0781-6156-52)
  • 75 mL in 1 BOTTLE (0781-6156-57)
source: ndc

Packages (3)

0781-6156-46 100 mL in 1 BOTTLE (0781-6156-46) 0781-6156-52 50 mL in 1 BOTTLE (0781-6156-52) 0781-6156-57 75 mL in 1 BOTTLE (0781-6156-57)

Ingredients (1)

amoxicillin (200 mg/5mL)

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 mL in 1 BOTTLE (0781-6156-46)", "package_ndc": "0781-6156-46", "marketing_start_date": "20070326"}, {"sample": false, "description": "50 mL in 1 BOTTLE (0781-6156-52)", "package_ndc": "0781-6156-52", "marketing_start_date": "20070326"}, {"sample": false, "description": "75 mL in 1 BOTTLE (0781-6156-57)", "package_ndc": "0781-6156-57", "marketing_start_date": "20070326"}], "brand_name": "Amoxicillin", "product_id": "0781-6156_6aa02079-d11c-4d2f-acaf-9548dd9a7ed6", "dosage_form": "POWDER, FOR SUSPENSION", "pharm_class": ["Penicillin-class Antibacterial [EPC]", "Penicillins [CS]"], "product_ndc": "0781-6156", "generic_name": "Amoxicillin", "labeler_name": "Sandoz Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amoxicillin", "active_ingredients": [{"name": "AMOXICILLIN", "strength": "200 mg/5mL"}], "application_number": "ANDA065378", "marketing_category": "ANDA", "marketing_start_date": "20070326", "listing_expiration_date": "20261231"}