cephalexin
Generic: cephalexin
Labeler: proficient rx lpDrug Facts
Product Profile
Brand Name
cephalexin
Generic Name
cephalexin
Labeler
proficient rx lp
Dosage Form
FOR SUSPENSION
Routes
Active Ingredients
cephalexin 250 mg/5mL
Manufacturer
Identifiers & Regulatory
Product NDC
71205-553
Product ID
71205-553_ff4b7d77-f5bf-4286-a4a3-9bb13949ad35
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA065234
Listing Expiration
2026-12-31
Marketing Start
2017-09-06
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
71205553
Hyphenated Format
71205-553
Supplemental Identifiers
RxCUI
UPC
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
ANDA065234 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 250 mg/5mL
Packaging
- 100 mL in 1 BOTTLE (71205-553-00)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "ff4b7d77-f5bf-4286-a4a3-9bb13949ad35", "openfda": {"upc": ["0371205553005"], "unii": ["OBN7UDS42Y"], "rxcui": ["309113"], "spl_set_id": ["829244bd-93da-4a5a-a257-890cfec4c06d"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "100 mL in 1 BOTTLE (71205-553-00)", "package_ndc": "71205-553-00", "marketing_start_date": "20210407"}], "brand_name": "cephalexin", "product_id": "71205-553_ff4b7d77-f5bf-4286-a4a3-9bb13949ad35", "dosage_form": "FOR SUSPENSION", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "71205-553", "generic_name": "Cephalexin", "labeler_name": "Proficient Rx LP", "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": "20170906", "listing_expiration_date": "20261231"}