cephalexin

Generic: cephalexin

Labeler: pharma-c, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name cephalexin
Generic Name cephalexin
Labeler pharma-c, inc.
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

cephalexin 250 mg/1

Manufacturer
Pharma-C, Inc.

Identifiers & Regulatory

Product NDC 69778-930
Product ID 69778-930_5f2379e6-9041-4de6-83a2-f63fa36db0d9
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA065152
Listing Expiration 2026-12-31
Marketing Start 2010-10-15

Pharmacologic Class

Classes
cephalosporin antibacterial [epc] cephalosporins [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 69778930
Hyphenated Format 69778-930

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 ANDA065152 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 250 mg/1
source: ndc
Packaging
  • 500 CAPSULE in 1 BOTTLE, PLASTIC (69778-930-04)
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": "5f2379e6-9041-4de6-83a2-f63fa36db0d9", "openfda": {"unii": ["OBN7UDS42Y"], "rxcui": ["309112", "309114"], "spl_set_id": ["bf9a6c06-11fd-4fb7-9cf5-e8e787758c1c"], "manufacturer_name": ["Pharma-C, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 CAPSULE in 1 BOTTLE, PLASTIC (69778-930-04)", "package_ndc": "69778-930-04", "marketing_start_date": "20161011"}], "brand_name": "Cephalexin", "product_id": "69778-930_5f2379e6-9041-4de6-83a2-f63fa36db0d9", "dosage_form": "CAPSULE", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "69778-930", "generic_name": "Cephalexin", "labeler_name": "Pharma-C, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cephalexin", "active_ingredients": [{"name": "CEPHALEXIN", "strength": "250 mg/1"}], "application_number": "ANDA065152", "marketing_category": "ANDA", "marketing_start_date": "20101015", "listing_expiration_date": "20261231"}