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CEPORACIN 1 G — DIN 02060051

CEPHALOTHIN (CEPHALOTHIN SODIUM) : 1 G · MYLAN PHARMACEUTICALS ULC · POWDER FOR SOLUTION · wholesale supply in Canada

Health Canada status: CANCELLED POST MARKET

What is CEPORACIN?

CEPORACIN 1 G contains CEPHALOTHIN (CEPHALOTHIN SODIUM) : 1 G. It is listed in the Health Canada Drug Product Database under DIN 02060051, held by MYLAN PHARMACEUTICALS ULC, supplied as POWDER FOR SOLUTION for INTRAMUSCULAR ; INTRAVENOUS administration. Health Canada currently lists it as cancelled post market, status dated 03-Nov-2015. This Drug Identification Number is no longer authorized for sale in Canada, so Nexara does not supply it. The record is kept here because buyers still meet the number on old formularies, purchase orders and tender documents; Nexara can help identify an authorized alternative.

What is CEPORACIN used for?

Serious infections (respiratory, skin, GU, septicemia, meningitis, bone/joint) caused by susceptible strains. Perioperative prophylaxis to reduce postoperative infections.

Authorized indication as written in the Health Canada product monograph. For healthcare professionals and licensed purchasers; this is not medical advice.

Is there a generic Cefalotin in Canada, and who makes it?

Every market authorization holder with a Canadian DIN for this molecule, and how many of their listings Health Canada currently shows as marketed.

2 holders have a Canadian DIN containing Cefalotin, across 4 DINs, of which 0 are currently marketed. Marketed count is the number that matters: an approval that is not marketed cannot be bought.

Market authorization holderDINsMarketedBrand namesPosition
ELI LILLY CANADA INC30KEFLIN ADD-VANTAGE INJ 1GM/VIAL, KEFLIN NEUTRAL INJ 1GM, KEFLIN NEUTRAL INJ 2GM/VIALNo marketed DIN
MYLAN PHARMACEUTICALS ULC10CEPORACINNo marketed DIN

Health Canada’s Drug Product Database does not flag which listing is the originator and which are subsequent-entry products, so Nexara does not label them here. Interchangeability is determined provincially, not federally — confirm for your province before a formulary switch. Nexara can confirm which of these is actually obtainable, and on what lead time, per order.

How is it supplied and stored?

Pack configuration, storage class and the handling constraints that drive cold-chain planning. One DIN can cover more than one pack size, and the pack — not the DIN — is what gets priced, shipped and invoiced.

Strength on the label1 G
Dosage formPOWDER FOR SOLUTION
RouteINTRAMUSCULAR ; INTRAVENOUS
Pack configuration (monograph)1 g vials containing cephalothin sodium and sodium bicarbonate buffer.
StorageReconstituted: 24h at room temperature or 72h refrigerated. Bacteriostatic I.M. solutions: 7 days refrigerated. Replace I.V. infusions every 24h. Do not use dark brown solutions.
Shipping classCold chain — validated shipper with temperature monitoring

Pack detail is kept as a regulatory record. This DIN is no longer authorized for sale in Canada, so Nexara does not quote this pack.

Substance and classification

Active substanceCefalotin
ATC codeJ01DB03
AHFS class08:12.06.04
Biosimilar biologicNo

Health Canada record and identifiers

The regulatory facts straight from the Drug Product Database, plus every identifier form Nexara accepts on a purchase order. A DIN written without its leading zeros is the commonest reason an order line fails to match.

DIN (8-digit, as used in ordering)02060051
DIN (unpadded, as printed on some documents)2060051
Brand nameCEPORACIN
Generic / active ingredientCEPHALOTHIN (CEPHALOTHIN SODIUM) : 1 G
Market authorization holderMYLAN PHARMACEUTICALS ULC
Health Canada schedulePrescription
ATC codeJ01DB03
ATC anatomical main groupJ — Anti-infectives for systemic use
ATC therapeutic subgroupJ01DB
Current statusCANCELLED POST MARKET
Status date03-Nov-2015
Original market date1994-12-31 00:00:00
Status sourceLive Health Canada DPD sync

Verify on the primary sources

Health Canada DPD record Approved product monograph (PDF)

How is it administered?

Adults: 500 mg to 2 g every 4 to 6 hours. Life-threatening: up to 2 g every 4 hours. Children: 80 to 160 mg/kg/day in divided doses. Administer via I.M., I.V. (bolus or infusion), or intraperitoneal.

Included because it drives pack selection and wastage. Consult the monograph.

Contraindications

Contraindicated in persons hypersensitive to the cephalosporins.

Warnings and precautions

Inquire about penicillin/cephalosporin allergy (cross-allergenicity risk). Pseudomembranous colitis risk. High I.V. doses (>6g/day) may cause thrombophlebitis. Seizure risk in renal impairment.

What can be used instead?

Alternatives on every axis a buyer actually considers — the same molecule in another presentation, the same class, an adjacent class, or a fixed-dose combination. Every row is led by the marketed DIN count, because that is what can be bought this week.

1 · Same molecule, other Canadian presentations

0 of 4 Canadian DINs for this molecule are currently marketed. Marketed products are listed first.

ProductStrengthFormHolderHealth Canada statusDIN
KEFLIN ADD-VANTAGE INJ 1GM/VIAL1 GLIQUIDELI LILLY CANADA INCCANCELLED POST MARKET00752525
KEFLIN NEUTRAL INJ 1GM1 GPOWDER FOR SOLUTIONELI LILLY CANADA INCCANCELLED POST MARKET00015369
KEFLIN NEUTRAL INJ 2GM/VIAL2 GPOWDER FOR SOLUTIONELI LILLY CANADA INCCANCELLED POST MARKET00244406

2 · Same class — other molecules in ATC J01DB

MoleculeCanadian brandsDINsMarketedSourceable
CefalexinAPO-CEPHALEX · ASN-CEPHALEXIN · AURO-CEPHALEXIN · CEPHALEXIN · +25 more4723Yes
CefazolinANCEF INJ PWS 10GM/VIAL USP · ANCEF INJ PWS 1GM/VIAL USP · ANCEF INJ PWS 500MG/VIAL USP · CEFAZOLIN FOR INJECTION · +8 more3415Yes
CefadroxilAPO-CEFADROXIL · CEFADROXIL · DURICEF · JAMP CEFADROXIL · +2 more63Yes
CefalotinCEPORACIN · KEFLIN ADD-VANTAGE INJ 1GM/VIAL · KEFLIN NEUTRAL INJ 1GM · KEFLIN NEUTRAL INJ 2GM/VIAL40Not in Canada

A molecule with zero marketed DINs cannot be sourced domestically, however many approvals it holds — if one of these sits on a formulary or in an older protocol, that is the line to check.

3 · Adjacent classes in ATC J01D

ATC subgroupMoleculesDINsMarketed
J01DDCefixime · Cefotaxime · Cefpodoxime · Ceftazidime · Ceftizoxime · +1 more9625
J01DHDoripenem · Ertapenem · Imipenem And Cilastatin · Meropenem · Meropenem And Vaborbactam5124
J01DCCefaclor · Cefamandole · Cefotetan · Cefoxitin · Cefprozil · +1 more13518
J01DECefepime103
J01DFAztreonam11
J01DICeftobiprole Medocaril · Ceftolozane And Beta-Lactamase Inhibitor21

Not clinical advice. These tables describe what can be supplied in Canada, not what should be prescribed. Substitution within or across classes is a prescriber and pharmacist decision, and interchangeability is determined provincially.

Can this still be bought in Canada?

No. This Drug Identification Number is cancelled post market in Health Canada's Drug Product Database, so the product is no longer authorized for sale in Canada and Nexara does not supply it. This page is kept as a regulatory record.

If you are looking for a current equivalent, the alternatives above list every product sharing this therapeutic class, with the marketed ones first. Ask us to source an alternative

Ordering questions

Who can buy this from Nexara?

Licensed entities only. Nexara holds Health Canada establishment licence DEL 3-002896-A and ships only to a licensed address. Patients and unlicensed buyers are routed to a partner pharmacy.

Is there a minimum order?

Yes, set per product line and per pack multiple rather than on the order total, so you are never asked to buy a part-pack. The minimum for this line is confirmed with your quote.

What is the lead time?

Confirmed per order at quotation, and it depends on current stock position and whether the product is in shortage.

Why is there no price on this page?

Nexara quotes a delivered Canadian price per order, against a verified licence. Foreign list prices are published on incompatible bases and are not a guide to what any buyer can obtain here, so this page shows which markets list the molecule and on what basis, and nothing more.

Can Nexara supply this for a clinical trial?

Yes — comparator and background-therapy supply, including sourcing from other markets where a Canadian pack will not satisfy the protocol. Clinical trial supply.

Sources and disclaimer

Product data sourced from the Health Canada Drug Product Database and the approved product monograph (PDF). Health Canada status reconciled against the live DPD sync. Last reviewed 10 Sep 2026.

Nothing on this page is medical advice. Nexara Health is a licensed wholesale distributor and supplies licensed entities only; consumer orders are routed to a partner pharmacy. Alternatives tables describe supply, not clinical equivalence.

Health Canada Drug Product Database (DPD), DIN 02060051. Last reviewed 2026-09-10. Nexara Health is a licensed wholesaler and supplies licensed entities only; consumer orders are routed to a partner pharmacy.