cephalexin

Generic: cephalexin

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

Drug Facts

Product Profile

Brand Name cephalexin
Generic Name cephalexin
Labeler qpharma inc
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

cephalexin 500 mg/1

Manufacturer
QPharma Inc

Identifiers & Regulatory

Product NDC 42708-070
Product ID 42708-070_45b3d102-f62e-5324-e063-6394a90a2f78
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA090836
Listing Expiration 2026-12-31
Marketing Start 2011-01-19

Pharmacologic Class

Classes
cephalosporin antibacterial [epc] cephalosporins [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 42708070
Hyphenated Format 42708-070

Supplemental Identifiers

RxCUI
309114
UNII
OBN7UDS42Y

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 ANDA090836 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 500 mg/1
source: ndc
Packaging
  • 28 CAPSULE in 1 BOTTLE (42708-070-28)
source: ndc

Packages (1)

42708-070-28 28 CAPSULE in 1 BOTTLE (42708-070-28)

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": "45b3d102-f62e-5324-e063-6394a90a2f78", "openfda": {"unii": ["OBN7UDS42Y"], "rxcui": ["309114"], "spl_set_id": ["a9d2e29e-9c3f-429d-9d22-481807becd33"], "manufacturer_name": ["QPharma Inc"]}, "finished": true, "packaging": [{"sample": true, "description": "28 CAPSULE in 1 BOTTLE (42708-070-28)", "package_ndc": "42708-070-28", "marketing_start_date": "20180918"}], "brand_name": "Cephalexin", "product_id": "42708-070_45b3d102-f62e-5324-e063-6394a90a2f78", "dosage_form": "CAPSULE", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "42708-070", "generic_name": "Cephalexin", "labeler_name": "QPharma Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cephalexin", "active_ingredients": [{"name": "CEPHALEXIN", "strength": "500 mg/1"}], "application_number": "ANDA090836", "marketing_category": "ANDA", "marketing_start_date": "20110119", "listing_expiration_date": "20261231"}