cefotan
Generic: cefotetan
Labeler: pai holdings, llc dba pai pharmaDrug Facts
Product Profile
Brand Name
cefotan
Generic Name
cefotetan
Labeler
pai holdings, llc dba pai pharma
Dosage Form
INJECTION, POWDER, FOR SOLUTION
Routes
Active Ingredients
cefotetan disodium 2 g/20mL
Manufacturer
Identifiers & Regulatory
Product NDC
0121-0977
Product ID
0121-0977_7e29cb53-c401-49b0-9b47-209601f7ec55
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
NDA
Application Number
NDA050588
Listing Expiration
2026-12-31
Marketing Start
2024-04-08
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
01210977
Hyphenated Format
0121-0977
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
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
cefotan (source: ndc)
Generic Name
cefotetan (source: ndc)
Application Number
NDA050588 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 2 g/20mL
Packaging
- 10 VIAL in 1 TRAY (0121-0977-10) / 20 mL in 1 VIAL (0121-0977-55)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "7e29cb53-c401-49b0-9b47-209601f7ec55", "openfda": {"unii": ["0GXP746VXB"], "rxcui": ["1722919", "1722921", "1731542", "1743557"], "spl_set_id": ["f1510f5e-d001-44e0-accb-27cf79fd4f9a"], "manufacturer_name": ["PAI Holdings, LLC dba PAI Pharma"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL in 1 TRAY (0121-0977-10) / 20 mL in 1 VIAL (0121-0977-55)", "package_ndc": "0121-0977-10", "marketing_start_date": "20240408"}], "brand_name": "Cefotan", "product_id": "0121-0977_7e29cb53-c401-49b0-9b47-209601f7ec55", "dosage_form": "INJECTION, POWDER, FOR SOLUTION", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "0121-0977", "generic_name": "Cefotetan", "labeler_name": "PAI Holdings, LLC dba PAI Pharma", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cefotan", "active_ingredients": [{"name": "CEFOTETAN DISODIUM", "strength": "2 g/20mL"}], "application_number": "NDA050588", "marketing_category": "NDA", "marketing_start_date": "20240408", "listing_expiration_date": "20261231"}