cephalexin

Generic: cephalexin

Labeler: aurobindo pharma limited
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name cephalexin
Generic Name cephalexin
Labeler aurobindo pharma limited
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

cephalexin 500 mg/1

Manufacturer
Aurobindo Pharma Limited

Identifiers & Regulatory

Product NDC 59651-784
Product ID 59651-784_e46059e1-3ce9-4a3c-80ce-464b140600ce
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA218817
Listing Expiration 2026-12-31
Marketing Start 2024-09-27

Pharmacologic Class

Classes
cephalosporin antibacterial [epc] cephalosporins [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 59651784
Hyphenated Format 59651-784

Supplemental Identifiers

RxCUI
197454 309115
UNII
OBN7UDS42Y

Packaging Origin

Original Packager
true

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 cephalexin (source: ndc)
Generic Name cephalexin (source: ndc)
Application Number ANDA218817 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 500 mg/1
source: ndc
Packaging
  • 100 TABLET, FILM COATED in 1 BOTTLE (59651-784-01)
source: ndc

Packages (1)

59651-784-01 100 TABLET, FILM COATED in 1 BOTTLE (59651-784-01)

Ingredients (1)

cephalexin (500 mg/1)

Linked Drug Pages (1)

Cephalexin ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "e46059e1-3ce9-4a3c-80ce-464b140600ce", "openfda": {"unii": ["OBN7UDS42Y"], "rxcui": ["197454", "309115"], "spl_set_id": ["e46059e1-3ce9-4a3c-80ce-464b140600ce"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (59651-784-01)", "package_ndc": "59651-784-01", "marketing_start_date": "20240927"}], "brand_name": "Cephalexin", "product_id": "59651-784_e46059e1-3ce9-4a3c-80ce-464b140600ce", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "59651-784", "generic_name": "Cephalexin", "labeler_name": "Aurobindo Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cephalexin", "active_ingredients": [{"name": "CEPHALEXIN", "strength": "500 mg/1"}], "application_number": "ANDA218817", "marketing_category": "ANDA", "marketing_start_date": "20240927", "listing_expiration_date": "20261231"}