amoxicillin

Generic: amoxicillin

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

Drug Facts

Product Profile

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

amoxicillin 875 mg/1

Manufacturer
REMEDYREPACK INC.

Identifiers & Regulatory

Product NDC 70518-2191
Product ID 70518-2191_49dbf57d-96d4-d3d6-e063-6394a90ac2d3
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA065256
Listing Expiration 2027-12-31
Marketing Start 2019-07-09

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 705182191
Hyphenated Format 70518-2191

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 ANDA065256 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 875 mg/1
source: ndc
Packaging
  • 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-2191-1)
  • 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-2191-2)
  • 14 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-2191-3)
  • 14 TABLET, FILM COATED in 1 BLISTER PACK (70518-2191-4)
source: ndc

Packages (4)

70518-2191-1 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-2191-1) 70518-2191-2 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-2191-2) 70518-2191-3 14 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-2191-3) 70518-2191-4 14 TABLET, FILM COATED in 1 BLISTER PACK (70518-2191-4)

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": "49dbf57d-96d4-d3d6-e063-6394a90ac2d3", "openfda": {"unii": ["804826J2HU"], "rxcui": ["308194"], "spl_set_id": ["9618d038-e880-47f6-b8d7-bbf8ab35364d"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (70518-2191-1)", "package_ndc": "70518-2191-1", "marketing_start_date": "20190709"}, {"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-2191-2)", "package_ndc": "70518-2191-2", "marketing_start_date": "20190719"}, {"sample": false, "description": "14 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-2191-3)", "package_ndc": "70518-2191-3", "marketing_start_date": "20190719"}, {"sample": false, "description": "14 TABLET, FILM COATED in 1 BLISTER PACK (70518-2191-4)", "package_ndc": "70518-2191-4", "marketing_start_date": "20200708"}], "brand_name": "Amoxicillin", "product_id": "70518-2191_49dbf57d-96d4-d3d6-e063-6394a90ac2d3", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Penicillin-class Antibacterial [EPC]", "Penicillins [CS]"], "product_ndc": "70518-2191", "generic_name": "Amoxicillin", "labeler_name": "REMEDYREPACK 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": "20190709", "listing_expiration_date": "20271231"}