cephalexin
Generic: cephalexin
Labeler: a-s medication solutionsDrug Facts
Product Profile
Brand Name
cephalexin
Generic Name
cephalexin
Labeler
a-s medication solutions
Dosage Form
CAPSULE
Routes
Active Ingredients
cephalexin 500 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
50090-7162
Product ID
50090-7162_4f68a97c-9fb2-4008-a541-e58c38910360
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA062702
Listing Expiration
2026-12-31
Marketing Start
1990-09-30
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
500907162
Hyphenated Format
50090-7162
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
ANDA062702 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 500 mg/1
Packaging
- 28 CAPSULE in 1 BOTTLE (50090-7162-1)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4f68a97c-9fb2-4008-a541-e58c38910360", "openfda": {"unii": ["OBN7UDS42Y"], "rxcui": ["309114"], "spl_set_id": ["5b7666f3-4014-45ce-8387-3298d9fe6d25"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "28 CAPSULE in 1 BOTTLE (50090-7162-1)", "package_ndc": "50090-7162-1", "marketing_start_date": "20240506"}], "brand_name": "Cephalexin", "product_id": "50090-7162_4f68a97c-9fb2-4008-a541-e58c38910360", "dosage_form": "CAPSULE", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "50090-7162", "generic_name": "Cephalexin", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cephalexin", "active_ingredients": [{"name": "CEPHALEXIN", "strength": "500 mg/1"}], "application_number": "ANDA062702", "marketing_category": "ANDA", "marketing_start_date": "19900930", "listing_expiration_date": "20261231"}