cephalexin

Generic: cephalexin

Labeler: ascend laboratories, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name cephalexin
Generic Name cephalexin
Labeler ascend laboratories, llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

cephalexin 250 mg/1

Manufacturer
Ascend Laboratories, LLC

Identifiers & Regulatory

Product NDC 67877-891
Product ID 67877-891_779b70b9-d16c-4421-9e45-7800e947690d
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA218947
Listing Expiration 2026-12-31
Marketing Start 2024-10-21

Pharmacologic Class

Classes
cephalosporin antibacterial [epc] cephalosporins [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 67877891
Hyphenated Format 67877-891

Supplemental Identifiers

RxCUI
197454 309115
UPC
0367877892849
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 ANDA218947 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 250 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (67877-891-01)
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": "779b70b9-d16c-4421-9e45-7800e947690d", "openfda": {"upc": ["0367877892849"], "unii": ["OBN7UDS42Y"], "rxcui": ["197454", "309115"], "spl_set_id": ["36882c6d-7b6f-41e3-8c54-e3b0073b8c07"], "manufacturer_name": ["Ascend Laboratories, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (67877-891-01)", "package_ndc": "67877-891-01", "marketing_start_date": "20241021"}], "brand_name": "Cephalexin", "product_id": "67877-891_779b70b9-d16c-4421-9e45-7800e947690d", "dosage_form": "TABLET", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "67877-891", "generic_name": "Cephalexin", "labeler_name": "Ascend Laboratories, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cephalexin", "active_ingredients": [{"name": "CEPHALEXIN", "strength": "250 mg/1"}], "application_number": "ANDA218947", "marketing_category": "ANDA", "marketing_start_date": "20241021", "listing_expiration_date": "20261231"}