cephalexin

Generic: cephalexin

Labeler: pd-rx pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name cephalexin
Generic Name cephalexin
Labeler pd-rx pharmaceuticals, inc.
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

cephalexin 500 mg/1

Manufacturer
PD-Rx Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 72789-251
Product ID 72789-251_40ad376a-ff01-ce39-e063-6294a90a7174
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA090836
Listing Expiration 2026-12-31
Marketing Start 2011-01-19

Pharmacologic Class

Classes
cephalosporin antibacterial [epc] cephalosporins [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72789251
Hyphenated Format 72789-251

Supplemental Identifiers

RxCUI
309114
UPC
0372789251820
UNII
OBN7UDS42Y

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
  • 500 mg/1
source: ndc
Packaging
  • 500 CAPSULE in 1 BOTTLE, PLASTIC (72789-251-82)
source: ndc

Packages (1)

Ingredients (1)

cephalexin (500 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "40ad376a-ff01-ce39-e063-6294a90a7174", "openfda": {"upc": ["0372789251820"], "unii": ["OBN7UDS42Y"], "rxcui": ["309114"], "spl_set_id": ["e54df878-c235-4aa3-af33-fe5287c73138"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "500 CAPSULE in 1 BOTTLE, PLASTIC (72789-251-82)", "package_ndc": "72789-251-82", "marketing_start_date": "20220517"}], "brand_name": "Cephalexin", "product_id": "72789-251_40ad376a-ff01-ce39-e063-6294a90a7174", "dosage_form": "CAPSULE", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "72789-251", "generic_name": "Cephalexin", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "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": "20110119", "listing_expiration_date": "20261231"}