cephalexin
Generic: cephalexin
Labeler: bryant ranch prepackDrug Facts
Product Profile
Brand Name
cephalexin
Generic Name
cephalexin
Labeler
bryant ranch prepack
Dosage Form
FOR SUSPENSION
Routes
Active Ingredients
cephalexin 250 mg/5mL
Manufacturer
Identifiers & Regulatory
Product NDC
71335-2734
Product ID
71335-2734_20b7a536-9dca-4a22-af63-ff82f1163153
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA210221
Listing Expiration
2026-12-31
Marketing Start
2019-03-28
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
713352734
Hyphenated Format
71335-2734
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
- 250 mg/5mL
Packaging
- 100 mL in 1 BOTTLE (71335-2734-1)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "20b7a536-9dca-4a22-af63-ff82f1163153", "openfda": {"unii": ["OBN7UDS42Y"], "rxcui": ["309113"], "spl_set_id": ["1bfa8744-24ee-4c70-845c-c532b8084433"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 mL in 1 BOTTLE (71335-2734-1)", "package_ndc": "71335-2734-1", "marketing_start_date": "20250729"}], "brand_name": "Cephalexin", "product_id": "71335-2734_20b7a536-9dca-4a22-af63-ff82f1163153", "dosage_form": "FOR SUSPENSION", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "71335-2734", "generic_name": "Cephalexin", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cephalexin", "active_ingredients": [{"name": "CEPHALEXIN", "strength": "250 mg/5mL"}], "application_number": "ANDA210221", "marketing_category": "ANDA", "marketing_start_date": "20190328", "listing_expiration_date": "20261231"}