cephalexin
Generic: cephalexin
Labeler: avkareDrug Facts
Product Profile
Brand Name
cephalexin
Generic Name
cephalexin
Labeler
avkare
Dosage Form
CAPSULE
Routes
Active Ingredients
cephalexin 250 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
42291-208
Product ID
42291-208_3a9ef551-6c16-2d5f-e063-6294a90a5130
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA062713
Listing Expiration
2026-12-31
Marketing Start
2011-08-11
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
42291208
Hyphenated Format
42291-208
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
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
ANDA062713 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 250 mg/1
Packaging
- 500 CAPSULE in 1 BOTTLE (42291-208-50)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3a9ef551-6c16-2d5f-e063-6294a90a5130", "openfda": {"unii": ["OBN7UDS42Y"], "rxcui": ["309112", "309114"], "spl_set_id": ["03f6f6ae-66bc-6819-8ba9-7c9c3fbef90d"], "manufacturer_name": ["AvKARE"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 CAPSULE in 1 BOTTLE (42291-208-50)", "package_ndc": "42291-208-50", "marketing_start_date": "20110811"}], "brand_name": "Cephalexin", "product_id": "42291-208_3a9ef551-6c16-2d5f-e063-6294a90a5130", "dosage_form": "CAPSULE", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "42291-208", "generic_name": "Cephalexin", "labeler_name": "AvKARE", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cephalexin", "active_ingredients": [{"name": "CEPHALEXIN", "strength": "250 mg/1"}], "application_number": "ANDA062713", "marketing_category": "ANDA", "marketing_start_date": "20110811", "listing_expiration_date": "20261231"}