cephalexin
Generic: cephalexin
Labeler: preferred pharmaceuticlas inc.Drug Facts
Product Profile
Brand Name
cephalexin
Generic Name
cephalexin
Labeler
preferred pharmaceuticlas inc.
Dosage Form
FOR SUSPENSION
Routes
Active Ingredients
cephalexin 125 mg/5mL
Manufacturer
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
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
687887796
Hyphenated Format
68788-7796
Supplemental Identifiers
RxCUI
UNII
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
source: ndc
Resolved Composition
Strengths
- 125 mg/5mL
Packaging
- 100 mL in 1 BOTTLE (68788-7796-1)
- 200 mL in 1 BOTTLE (68788-7796-2)
Packages (2)
Ingredients (1)
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"}