cephalexin

Generic: cephalexin

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

Drug Facts

Product Profile

Brand Name cephalexin
Generic Name cephalexin
Labeler nucare pharmaceuticals,inc.
Dosage Form POWDER, FOR SUSPENSION
Routes
ORAL
Active Ingredients

cephalexin 250 mg/5mL

Manufacturer
NuCare Pharmaceuticals,Inc.

Identifiers & Regulatory

Product NDC 66267-982
Product ID 66267-982_1fa7ce69-a972-59e7-e063-6394a90af771
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA062703
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 66267982
Hyphenated Format 66267-982

Supplemental Identifiers

RxCUI
309113
UPC
0366267982009
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 ANDA062703 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 250 mg/5mL
source: ndc
Packaging
  • 100 mL in 1 BOTTLE (66267-982-00)
source: ndc

Packages (1)

66267-982-00 100 mL in 1 BOTTLE (66267-982-00)

Ingredients (1)

cephalexin (250 mg/5mL)

Linked Drug Pages (1)

Cephalexin ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "1fa7ce69-a972-59e7-e063-6394a90af771", "openfda": {"upc": ["0366267982009"], "unii": ["OBN7UDS42Y"], "rxcui": ["309113"], "spl_set_id": ["549bf887-1ef6-6a75-e054-00144ff8d46c"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 mL in 1 BOTTLE (66267-982-00)", "package_ndc": "66267-982-00", "marketing_start_date": "20170718"}], "brand_name": "Cephalexin", "product_id": "66267-982_1fa7ce69-a972-59e7-e063-6394a90af771", "dosage_form": "POWDER, FOR SUSPENSION", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "66267-982", "generic_name": "Cephalexin", "labeler_name": "NuCare Pharmaceuticals,Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cephalexin", "active_ingredients": [{"name": "CEPHALEXIN", "strength": "250 mg/5mL"}], "application_number": "ANDA062703", "marketing_category": "ANDA", "marketing_start_date": "19900930", "listing_expiration_date": "20261231"}