amoxicillin

Generic: amoxicillin

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

Drug Facts

Product Profile

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

amoxicillin 875 mg/1

Manufacturer
QPharma, Inc.

Identifiers & Regulatory

Product NDC 42708-112
Product ID 42708-112_4682c86c-a853-ade0-e063-6394a90acbce
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA065056
Listing Expiration 2026-12-31
Marketing Start 2000-09-26

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 42708112
Hyphenated Format 42708-112

Supplemental Identifiers

RxCUI
308194
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 ANDA065056 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 875 mg/1
source: ndc
Packaging
  • 20 TABLET, FILM COATED in 1 BOTTLE (42708-112-20)
source: ndc

Packages (1)

42708-112-20 20 TABLET, FILM COATED in 1 BOTTLE (42708-112-20)

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": "4682c86c-a853-ade0-e063-6394a90acbce", "openfda": {"unii": ["804826J2HU"], "rxcui": ["308194"], "spl_set_id": ["7f40b439-d826-4a19-b184-702e9bd5a883"], "manufacturer_name": ["QPharma, Inc."]}, "finished": true, "packaging": [{"sample": true, "description": "20 TABLET, FILM COATED in 1 BOTTLE (42708-112-20)", "package_ndc": "42708-112-20", "marketing_start_date": "20180417"}], "brand_name": "Amoxicillin", "product_id": "42708-112_4682c86c-a853-ade0-e063-6394a90acbce", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Penicillin-class Antibacterial [EPC]", "Penicillins [CS]"], "product_ndc": "42708-112", "generic_name": "Amoxicillin", "labeler_name": "QPharma, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amoxicillin", "active_ingredients": [{"name": "AMOXICILLIN", "strength": "875 mg/1"}], "application_number": "ANDA065056", "marketing_category": "ANDA", "marketing_start_date": "20000926", "listing_expiration_date": "20261231"}