cephalexin

Generic: cephalexin

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

Drug Facts

Product Profile

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

cephalexin 125 mg/5mL

Manufacturer
Preferred Pharmaceuticlas Inc.

Identifiers & Regulatory

Product NDC 68788-7796
Product ID 68788-7796_f24e71f0-34a4-4e75-a398-e22e633f6413
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA210221
Listing Expiration 2026-12-31
Marketing Start 2020-10-13

Pharmacologic Class

Classes
cephalosporin antibacterial [epc] cephalosporins [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 687887796
Hyphenated Format 68788-7796

Supplemental Identifiers

RxCUI
309110
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 ANDA210221 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 125 mg/5mL
source: ndc
Packaging
  • 100 mL in 1 BOTTLE (68788-7796-1)
  • 200 mL in 1 BOTTLE (68788-7796-2)
source: ndc

Packages (2)

Ingredients (1)

cephalexin (125 mg/5mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "f24e71f0-34a4-4e75-a398-e22e633f6413", "openfda": {"unii": ["OBN7UDS42Y"], "rxcui": ["309110"], "spl_set_id": ["fbf5fcdf-40fc-40e5-b784-308032fff0e5"], "manufacturer_name": ["Preferred Pharmaceuticlas Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 mL in 1 BOTTLE (68788-7796-1)", "package_ndc": "68788-7796-1", "marketing_start_date": "20201013"}, {"sample": false, "description": "200 mL in 1 BOTTLE (68788-7796-2)", "package_ndc": "68788-7796-2", "marketing_start_date": "20201013"}], "brand_name": "Cephalexin", "product_id": "68788-7796_f24e71f0-34a4-4e75-a398-e22e633f6413", "dosage_form": "FOR SUSPENSION", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "68788-7796", "generic_name": "Cephalexin", "labeler_name": "Preferred Pharmaceuticlas Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cephalexin", "active_ingredients": [{"name": "CEPHALEXIN", "strength": "125 mg/5mL"}], "application_number": "ANDA210221", "marketing_category": "ANDA", "marketing_start_date": "20201013", "listing_expiration_date": "20261231"}