amoxicillin

Generic: amoxicillin

Labeler: proficient rx lp
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name amoxicillin
Generic Name amoxicillin
Labeler proficient rx lp
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

amoxicillin 875 mg/1

Manufacturer
Proficient Rx LP

Identifiers & Regulatory

Product NDC 71205-035
Product ID 71205-035_23c32fbb-0d4d-4830-883f-0967c8586247
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA065228
Listing Expiration 2026-12-31
Marketing Start 2005-07-13

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 71205035
Hyphenated Format 71205-035

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 ANDA065228 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 875 mg/1
source: ndc
Packaging
  • 14 TABLET, FILM COATED in 1 BOTTLE (71205-035-14)
  • 20 TABLET, FILM COATED in 1 BOTTLE (71205-035-20)
  • 30 TABLET, FILM COATED in 1 BOTTLE (71205-035-30)
  • 60 TABLET, FILM COATED in 1 BOTTLE (71205-035-60)
  • 90 TABLET, FILM COATED in 1 BOTTLE (71205-035-90)
source: ndc

Packages (5)

71205-035-14 14 TABLET, FILM COATED in 1 BOTTLE (71205-035-14) 71205-035-20 20 TABLET, FILM COATED in 1 BOTTLE (71205-035-20) 71205-035-30 30 TABLET, FILM COATED in 1 BOTTLE (71205-035-30) 71205-035-60 60 TABLET, FILM COATED in 1 BOTTLE (71205-035-60) 71205-035-90 90 TABLET, FILM COATED in 1 BOTTLE (71205-035-90)

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": "23c32fbb-0d4d-4830-883f-0967c8586247", "openfda": {"unii": ["804826J2HU"], "rxcui": ["308194"], "spl_set_id": ["7974a666-6d1d-446b-8ea5-f7145dc66358"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "14 TABLET, FILM COATED in 1 BOTTLE (71205-035-14)", "package_ndc": "71205-035-14", "marketing_start_date": "20190901"}, {"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE (71205-035-20)", "package_ndc": "71205-035-20", "marketing_start_date": "20180501"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71205-035-30)", "package_ndc": "71205-035-30", "marketing_start_date": "20180501"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (71205-035-60)", "package_ndc": "71205-035-60", "marketing_start_date": "20180501"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (71205-035-90)", "package_ndc": "71205-035-90", "marketing_start_date": "20180501"}], "brand_name": "Amoxicillin", "product_id": "71205-035_23c32fbb-0d4d-4830-883f-0967c8586247", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Penicillin-class Antibacterial [EPC]", "Penicillins [CS]"], "product_ndc": "71205-035", "generic_name": "Amoxicillin", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amoxicillin", "active_ingredients": [{"name": "AMOXICILLIN", "strength": "875 mg/1"}], "application_number": "ANDA065228", "marketing_category": "ANDA", "marketing_start_date": "20050713", "listing_expiration_date": "20261231"}