cephalexin
Generic: cephalexin
Labeler: a-s medication solutionsDrug Facts
Product Profile
Brand Name
cephalexin
Generic Name
cephalexin
Labeler
a-s medication solutions
Dosage Form
FOR SUSPENSION
Routes
Active Ingredients
cephalexin 250 mg/5mL
Manufacturer
Identifiers & Regulatory
Product NDC
50090-7091
Product ID
50090-7091_90dcd7f5-e0f8-454d-89b5-2eedeff32e54
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
500907091
Hyphenated Format
50090-7091
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
ANDA065234 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 250 mg/5mL
Packaging
- 200 mL in 1 BOTTLE (50090-7091-0)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "90dcd7f5-e0f8-454d-89b5-2eedeff32e54", "openfda": {"unii": ["OBN7UDS42Y"], "rxcui": ["309113"], "spl_set_id": ["d31da5be-c939-4aa0-adb8-b26a1396b228"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "200 mL in 1 BOTTLE (50090-7091-0)", "package_ndc": "50090-7091-0", "marketing_start_date": "20240212"}], "brand_name": "cephalexin", "product_id": "50090-7091_90dcd7f5-e0f8-454d-89b5-2eedeff32e54", "dosage_form": "FOR SUSPENSION", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "50090-7091", "generic_name": "Cephalexin", "labeler_name": "A-S Medication Solutions", "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"}