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 CAPSULE
Routes
ORAL
Active Ingredients

amoxicillin 500 mg/1

Manufacturer
QPharma Inc

Identifiers & Regulatory

Product NDC 42708-076
Product ID 42708-076_45b3bfb1-8029-5885-e063-6394a90a0c13
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA065271
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 42708076
Hyphenated Format 42708-076

Supplemental Identifiers

RxCUI
308191
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 ANDA065271 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 500 mg/1
source: ndc
Packaging
  • 30 CAPSULE in 1 BOTTLE (42708-076-30)
source: ndc

Packages (1)

42708-076-30 30 CAPSULE in 1 BOTTLE (42708-076-30)

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": "45b3bfb1-8029-5885-e063-6394a90a0c13", "openfda": {"unii": ["804826J2HU"], "rxcui": ["308191"], "spl_set_id": ["2772a745-1276-405b-b229-95edf5534b2a"], "manufacturer_name": ["QPharma Inc"]}, "finished": true, "packaging": [{"sample": true, "description": "30 CAPSULE in 1 BOTTLE (42708-076-30)", "package_ndc": "42708-076-30", "marketing_start_date": "20181218"}], "brand_name": "Amoxicillin", "product_id": "42708-076_45b3bfb1-8029-5885-e063-6394a90a0c13", "dosage_form": "CAPSULE", "pharm_class": ["Penicillin-class Antibacterial [EPC]", "Penicillins [CS]"], "product_ndc": "42708-076", "generic_name": "Amoxicillin", "labeler_name": "QPharma Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amoxicillin", "active_ingredients": [{"name": "AMOXICILLIN", "strength": "500 mg/1"}], "application_number": "ANDA065271", "marketing_category": "ANDA", "marketing_start_date": "20051109", "listing_expiration_date": "20261231"}