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 875 mg/1

Manufacturer
NuCare Pharmaceuticals,Inc.

Identifiers & Regulatory

Product NDC 68071-4982
Product ID 68071-4982_44fcbea4-7615-1d98-e063-6294a90a6b32
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 680714982
Hyphenated Format 68071-4982

Supplemental Identifiers

RxCUI
308194
UPC
0368071498226
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
  • 875 mg/1
source: ndc
Packaging
  • 20 TABLET, FILM COATED in 1 BOTTLE (68071-4982-2)
source: ndc

Packages (1)

68071-4982-2 20 TABLET, FILM COATED in 1 BOTTLE (68071-4982-2)

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": "44fcbea4-7615-1d98-e063-6294a90a6b32", "openfda": {"upc": ["0368071498226"], "unii": ["804826J2HU"], "rxcui": ["308194"], "spl_set_id": ["8e6f9df1-0754-69e4-e053-2a95a90acc49"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE (68071-4982-2)", "package_ndc": "68071-4982-2", "marketing_start_date": "20190724"}], "brand_name": "Amoxicillin", "product_id": "68071-4982_44fcbea4-7615-1d98-e063-6294a90a6b32", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Penicillin-class Antibacterial [EPC]", "Penicillins [CS]"], "product_ndc": "68071-4982", "generic_name": "Amoxicillin", "labeler_name": "NuCare Pharmaceuticals,Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amoxicillin", "active_ingredients": [{"name": "AMOXICILLIN", "strength": "875 mg/1"}], "application_number": "ANDA065256", "marketing_category": "ANDA", "marketing_start_date": "20051109", "listing_expiration_date": "20261231"}