cephalexin

Generic: cephalexin

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

Drug Facts

Product Profile

Brand Name cephalexin
Generic Name cephalexin
Labeler asclemed usa, inc.
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

cephalexin 250 mg/1

Manufacturer
Asclemed USA, Inc.

Identifiers & Regulatory

Product NDC 76420-034
Product ID 76420-034_e436e361-d938-7d6d-e053-2995a90a10e4
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA090836
Listing Expiration 2026-12-31
Marketing Start 2011-01-20

Pharmacologic Class

Classes
cephalosporin antibacterial [epc] cephalosporins [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 76420034
Hyphenated Format 76420-034

Supplemental Identifiers

RxCUI
309112
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
  • 250 mg/1
source: ndc
Packaging
  • 40 CAPSULE in 1 BOTTLE (76420-034-40)
source: ndc

Packages (1)

76420-034-40 40 CAPSULE in 1 BOTTLE (76420-034-40)

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": "e436e361-d938-7d6d-e053-2995a90a10e4", "openfda": {"unii": ["OBN7UDS42Y"], "rxcui": ["309112"], "spl_set_id": ["891b8c0e-dbf4-4b0e-ba3f-c4c49d51510d"], "manufacturer_name": ["Asclemed USA, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "40 CAPSULE in 1 BOTTLE (76420-034-40)", "package_ndc": "76420-034-40", "marketing_start_date": "20220720"}], "brand_name": "Cephalexin", "product_id": "76420-034_e436e361-d938-7d6d-e053-2995a90a10e4", "dosage_form": "CAPSULE", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "76420-034", "generic_name": "Cephalexin", "labeler_name": "Asclemed USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cephalexin", "active_ingredients": [{"name": "CEPHALEXIN", "strength": "250 mg/1"}], "application_number": "ANDA090836", "marketing_category": "ANDA", "marketing_start_date": "20110120", "listing_expiration_date": "20261231"}