cephalexin

Generic: cephalexin

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

Drug Facts

Product Profile

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

cephalexin 250 mg/5mL

Manufacturer
Preferred Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 68788-8686
Product ID 68788-8686_6994016d-9c09-45ad-b869-a8f62f8e0a80
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA065234
Listing Expiration 2026-12-31
Marketing Start 2024-06-03

Pharmacologic Class

Classes
cephalosporin antibacterial [epc] cephalosporins [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 687888686
Hyphenated Format 68788-8686

Supplemental Identifiers

RxCUI
309113
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 ANDA065234 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 250 mg/5mL
source: ndc
Packaging
  • 200 mL in 1 BOTTLE (68788-8686-2)
source: ndc

Packages (1)

68788-8686-2 200 mL in 1 BOTTLE (68788-8686-2)

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": "6994016d-9c09-45ad-b869-a8f62f8e0a80", "openfda": {"unii": ["OBN7UDS42Y"], "rxcui": ["309113"], "spl_set_id": ["553485f8-890d-4929-a6bb-905221cf411d"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "200 mL in 1 BOTTLE (68788-8686-2)", "package_ndc": "68788-8686-2", "marketing_start_date": "20240603"}], "brand_name": "cephalexin", "product_id": "68788-8686_6994016d-9c09-45ad-b869-a8f62f8e0a80", "dosage_form": "FOR SUSPENSION", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "68788-8686", "generic_name": "Cephalexin", "labeler_name": "Preferred Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "cephalexin", "active_ingredients": [{"name": "CEPHALEXIN", "strength": "250 mg/5mL"}], "application_number": "ANDA065234", "marketing_category": "ANDA", "marketing_start_date": "20240603", "listing_expiration_date": "20261231"}