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 CAPSULE
Routes
ORAL
Active Ingredients

cephalexin 500 mg/1

Manufacturer
REMEDYREPACK INC.

Identifiers & Regulatory

Product NDC 70518-3059
Product ID 70518-3059_47e06741-5144-ce01-e063-6294a90aae63
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA090836
Listing Expiration 2027-12-31
Marketing Start 2021-03-29

Pharmacologic Class

Classes
cephalosporin antibacterial [epc] cephalosporins [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 705183059
Hyphenated Format 70518-3059

Supplemental Identifiers

RxCUI
309114
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
  • 14 CAPSULE in 1 BOTTLE, PLASTIC (70518-3059-0)
  • 30 CAPSULE in 1 BLISTER PACK (70518-3059-1)
  • 20 CAPSULE in 1 BOTTLE, PLASTIC (70518-3059-2)
  • 21 CAPSULE in 1 BOTTLE, PLASTIC (70518-3059-4)
  • 30 CAPSULE in 1 BOTTLE, PLASTIC (70518-3059-7)
  • 28 CAPSULE in 1 BOTTLE, PLASTIC (70518-3059-8)
source: ndc

Packages (6)

70518-3059-0 14 CAPSULE in 1 BOTTLE, PLASTIC (70518-3059-0) 70518-3059-1 30 CAPSULE in 1 BLISTER PACK (70518-3059-1) 70518-3059-2 20 CAPSULE in 1 BOTTLE, PLASTIC (70518-3059-2) 70518-3059-4 21 CAPSULE in 1 BOTTLE, PLASTIC (70518-3059-4) 70518-3059-7 30 CAPSULE in 1 BOTTLE, PLASTIC (70518-3059-7) 70518-3059-8 28 CAPSULE in 1 BOTTLE, PLASTIC (70518-3059-8)

Ingredients (1)

cephalexin (500 mg/1)

Linked Drug Pages (1)

Cephalexin ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "47e06741-5144-ce01-e063-6294a90aae63", "openfda": {"unii": ["OBN7UDS42Y"], "rxcui": ["309114"], "spl_set_id": ["d3527c0a-94e4-46a2-be77-d936abcd19ec"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "14 CAPSULE in 1 BOTTLE, PLASTIC (70518-3059-0)", "package_ndc": "70518-3059-0", "marketing_start_date": "20210329"}, {"sample": false, "description": "30 CAPSULE in 1 BLISTER PACK (70518-3059-1)", "package_ndc": "70518-3059-1", "marketing_start_date": "20210329"}, {"sample": false, "description": "20 CAPSULE in 1 BOTTLE, PLASTIC (70518-3059-2)", "package_ndc": "70518-3059-2", "marketing_start_date": "20210408"}, {"sample": false, "description": "21 CAPSULE in 1 BOTTLE, PLASTIC (70518-3059-4)", "package_ndc": "70518-3059-4", "marketing_start_date": "20210923"}, {"sample": false, "description": "30 CAPSULE in 1 BOTTLE, PLASTIC (70518-3059-7)", "package_ndc": "70518-3059-7", "marketing_start_date": "20211014"}, {"sample": false, "description": "28 CAPSULE in 1 BOTTLE, PLASTIC (70518-3059-8)", "package_ndc": "70518-3059-8", "marketing_start_date": "20211122"}], "brand_name": "Cephalexin", "product_id": "70518-3059_47e06741-5144-ce01-e063-6294a90aae63", "dosage_form": "CAPSULE", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "70518-3059", "generic_name": "Cephalexin", "labeler_name": "REMEDYREPACK 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": "20210329", "listing_expiration_date": "20271231"}