cephalexin
Generic: cephalexin
Labeler: major pharmaceuticalsDrug Facts
Product Profile
Brand Name
cephalexin
Generic Name
cephalexin
Labeler
major pharmaceuticals
Dosage Form
CAPSULE
Routes
Active Ingredients
cephalexin 500 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
0904-7337
Product ID
0904-7337_1c1fbad7-bef4-42a0-a8c9-b35168f5d533
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA090836
Listing Expiration
2026-12-31
Marketing Start
2023-11-06
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
09047337
Hyphenated Format
0904-7337
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
ANDA090836 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 500 mg/1
Packaging
- 50 BLISTER PACK in 1 CARTON (0904-7337-06) / 1 CAPSULE in 1 BLISTER PACK
- 100 BLISTER PACK in 1 CARTON (0904-7337-61) / 1 CAPSULE in 1 BLISTER PACK
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "1c1fbad7-bef4-42a0-a8c9-b35168f5d533", "openfda": {"unii": ["OBN7UDS42Y"], "rxcui": ["309112", "309114"], "spl_set_id": ["1c1fbad7-bef4-42a0-a8c9-b35168f5d533"], "manufacturer_name": ["Major Pharmaceuticals"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "50 BLISTER PACK in 1 CARTON (0904-7337-06) / 1 CAPSULE in 1 BLISTER PACK", "package_ndc": "0904-7337-06", "marketing_start_date": "20231106"}, {"sample": false, "description": "100 BLISTER PACK in 1 CARTON (0904-7337-61) / 1 CAPSULE in 1 BLISTER PACK", "package_ndc": "0904-7337-61", "marketing_start_date": "20231106"}], "brand_name": "Cephalexin", "product_id": "0904-7337_1c1fbad7-bef4-42a0-a8c9-b35168f5d533", "dosage_form": "CAPSULE", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "0904-7337", "generic_name": "Cephalexin", "labeler_name": "Major Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cephalexin", "active_ingredients": [{"name": "CEPHALEXIN", "strength": "500 mg/1"}], "application_number": "ANDA090836", "marketing_category": "ANDA", "marketing_start_date": "20231106", "listing_expiration_date": "20261231"}