cephalexin

Generic: cephalexin

Labeler: remedyrepack inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name cephalexin
Generic Name cephalexin
Labeler remedyrepack inc.
Dosage Form FOR SUSPENSION
Routes
ORAL
Active Ingredients

cephalexin 250 mg/5mL

Manufacturer
REMEDYREPACK INC.

Identifiers & Regulatory

Product NDC 70518-4511
Product ID 70518-4511_42397ed1-11b3-2036-e063-6294a90adb46
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA210221
Listing Expiration 2026-12-31
Marketing Start 2025-10-28

Pharmacologic Class

Classes
cephalosporin antibacterial [epc] cephalosporins [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 705184511
Hyphenated Format 70518-4511

Supplemental Identifiers

RxCUI
309113
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 ANDA210221 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 250 mg/5mL
source: ndc
Packaging
  • 100 mL in 1 BOTTLE (70518-4511-0)
source: ndc

Packages (1)

70518-4511-0 100 mL in 1 BOTTLE (70518-4511-0)

Ingredients (1)

cephalexin (250 mg/5mL)

Linked Drug Pages (1)

Cephalexin ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "42397ed1-11b3-2036-e063-6294a90adb46", "openfda": {"unii": ["OBN7UDS42Y"], "rxcui": ["309113"], "spl_set_id": ["9fc5cfb0-7ba0-4669-b79c-270b6a9ff573"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "100 mL in 1 BOTTLE (70518-4511-0)", "package_ndc": "70518-4511-0", "marketing_start_date": "20251028"}], "brand_name": "Cephalexin", "product_id": "70518-4511_42397ed1-11b3-2036-e063-6294a90adb46", "dosage_form": "FOR SUSPENSION", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "70518-4511", "generic_name": "Cephalexin", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cephalexin", "active_ingredients": [{"name": "CEPHALEXIN", "strength": "250 mg/5mL"}], "application_number": "ANDA210221", "marketing_category": "ANDA", "marketing_start_date": "20251028", "listing_expiration_date": "20261231"}