cephalexin

Generic: cephalexin

Labeler: northwind pharmaceuticals, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name cephalexin
Generic Name cephalexin
Labeler northwind pharmaceuticals, llc
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

cephalexin 500 mg/1

Manufacturer
Northwind Pharmaceuticals, LLC

Identifiers & Regulatory

Product NDC 51655-028
Product ID 51655-028_4768d6e6-d4ee-0e49-e063-6394a90adbc9
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA090836
Marketing Start 2014-11-06
Marketing End 2026-08-31

Pharmacologic Class

Classes
cephalosporin antibacterial [epc] cephalosporins [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 51655028
Hyphenated Format 51655-028

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
  • 20 CAPSULE in 1 BOTTLE, DISPENSING (51655-028-20)
source: ndc

Packages (1)

Ingredients (1)

cephalexin (500 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4768d6e6-d4ee-0e49-e063-6394a90adbc9", "openfda": {"unii": ["OBN7UDS42Y"], "rxcui": ["309114"], "spl_set_id": ["89bb3920-69bf-4818-b573-4bd845f6e2d5"], "manufacturer_name": ["Northwind Pharmaceuticals, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "20 CAPSULE in 1 BOTTLE, DISPENSING (51655-028-20)", "package_ndc": "51655-028-20", "marketing_end_date": "20260831", "marketing_start_date": "20141106"}], "brand_name": "Cephalexin", "product_id": "51655-028_4768d6e6-d4ee-0e49-e063-6394a90adbc9", "dosage_form": "CAPSULE", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "51655-028", "generic_name": "Cephalexin", "labeler_name": "Northwind Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cephalexin", "active_ingredients": [{"name": "CEPHALEXIN", "strength": "500 mg/1"}], "application_number": "ANDA090836", "marketing_category": "ANDA", "marketing_end_date": "20260831", "marketing_start_date": "20141106"}