cephalexin

Generic: cephalexin

Labeler: major pharmaceuticals
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name cephalexin
Generic Name cephalexin
Labeler major pharmaceuticals
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

cephalexin 250 mg/1

Manufacturer
Major Pharmaceuticals

Identifiers & Regulatory

Product NDC 0904-7336
Product ID 0904-7336_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
cephalosporin antibacterial [epc] cephalosporins [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 09047336
Hyphenated Format 0904-7336

Supplemental Identifiers

RxCUI
309112 309114
UNII
OBN7UDS42Y

Packaging Origin

Original Packager
true

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
ORAL
source: ndc

Resolved Composition

Strengths
  • 250 mg/1
source: ndc
Packaging
  • 100 BLISTER PACK in 1 CARTON (0904-7336-61) / 1 CAPSULE in 1 BLISTER PACK
source: ndc

Packages (1)

Ingredients (1)

cephalexin (250 mg/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": "100 BLISTER PACK in 1 CARTON (0904-7336-61)  / 1 CAPSULE in 1 BLISTER PACK", "package_ndc": "0904-7336-61", "marketing_start_date": "20231106"}], "brand_name": "Cephalexin", "product_id": "0904-7336_1c1fbad7-bef4-42a0-a8c9-b35168f5d533", "dosage_form": "CAPSULE", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "0904-7336", "generic_name": "Cephalexin", "labeler_name": "Major Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cephalexin", "active_ingredients": [{"name": "CEPHALEXIN", "strength": "250 mg/1"}], "application_number": "ANDA090836", "marketing_category": "ANDA", "marketing_start_date": "20231106", "listing_expiration_date": "20261231"}