cephalexin

Generic: cephalexin

Labeler: teva pharmaceuticals usa, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name cephalexin
Generic Name cephalexin
Labeler teva pharmaceuticals usa, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

cephalexin 250 mg/1

Manufacturer
Teva Pharmaceuticals USA, Inc.

Identifiers & Regulatory

Product NDC 0093-2238
Product ID 0093-2238_39e510b0-2478-4e34-81a1-20f002a6ae35
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA063024
Listing Expiration 2026-12-31
Marketing Start 1990-09-30

Pharmacologic Class

Classes
cephalosporin antibacterial [epc] cephalosporins [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 00932238
Hyphenated Format 0093-2238

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 ANDA063024 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 250 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (0093-2238-01)
source: ndc

Packages (1)

0093-2238-01 100 TABLET in 1 BOTTLE (0093-2238-01)

Ingredients (1)

cephalexin (250 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": "39e510b0-2478-4e34-81a1-20f002a6ae35", "openfda": {"unii": ["OBN7UDS42Y"], "rxcui": ["197454", "309115"], "spl_set_id": ["445b2a87-2e4f-483a-abe8-26fefd67514a"], "manufacturer_name": ["Teva Pharmaceuticals USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (0093-2238-01)", "package_ndc": "0093-2238-01", "marketing_start_date": "19900930"}], "brand_name": "Cephalexin", "product_id": "0093-2238_39e510b0-2478-4e34-81a1-20f002a6ae35", "dosage_form": "TABLET", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "0093-2238", "generic_name": "Cephalexin", "labeler_name": "Teva Pharmaceuticals USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cephalexin", "active_ingredients": [{"name": "CEPHALEXIN", "strength": "250 mg/1"}], "application_number": "ANDA063024", "marketing_category": "ANDA", "marketing_start_date": "19900930", "listing_expiration_date": "20261231"}