amoxicillin

Generic: amoxicillin

Labeler: nucare pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

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

amoxicillin 500 mg/1

Manufacturer
NuCare Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 68071-3675
Product ID 68071-3675_20eb1df7-535e-a7bd-e063-6394a90ad98c
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA065256
Listing Expiration 2026-12-31
Marketing Start 2005-11-09

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 680713675
Hyphenated Format 68071-3675

Supplemental Identifiers

RxCUI
308192
UPC
0368071367522
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 ANDA065256 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 500 mg/1
source: ndc
Packaging
  • 20 TABLET, FILM COATED in 1 BOTTLE (68071-3675-2)
source: ndc

Packages (1)

68071-3675-2 20 TABLET, FILM COATED in 1 BOTTLE (68071-3675-2)

Ingredients (1)

amoxicillin (500 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": "20eb1df7-535e-a7bd-e063-6394a90ad98c", "openfda": {"upc": ["0368071367522"], "unii": ["804826J2HU"], "rxcui": ["308192"], "spl_set_id": ["20eb4ade-f3b8-db66-e063-6294a90ae846"], "manufacturer_name": ["NuCare Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE (68071-3675-2)", "package_ndc": "68071-3675-2", "marketing_start_date": "20240830"}], "brand_name": "Amoxicillin", "product_id": "68071-3675_20eb1df7-535e-a7bd-e063-6394a90ad98c", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Penicillin-class Antibacterial [EPC]", "Penicillins [CS]"], "product_ndc": "68071-3675", "generic_name": "Amoxicillin", "labeler_name": "NuCare Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amoxicillin", "active_ingredients": [{"name": "AMOXICILLIN", "strength": "500 mg/1"}], "application_number": "ANDA065256", "marketing_category": "ANDA", "marketing_start_date": "20051109", "listing_expiration_date": "20261231"}