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PHENOBARBITAL SODIUM INJECTION, USP 120 MG

PHENOBARBITAL SODIUM : 120 MG · DIN 02304090 · SANDOZ CANADA INCORPORATED

Health Canada status: MARKETED

What is PHENOBARBITAL SODIUM INJECTION, USP?

PHENOBARBITAL SODIUM INJECTION, USP 120 MG contains PHENOBARBITAL SODIUM : 120 MG. It is listed in the Health Canada Drug Product Database under DIN 02304090, held by SANDOZ CANADA INCORPORATED, supplied as SOLUTION for INTRAMUSCULAR ; INTRAVENOUS administration. Health Canada currently lists it as marketed, status dated 29-Feb-2008. Nexara Health is a licensed Canadian wholesale distributor (DEL 3-002896-A) and can source this product for hospitals, pharmacies and clinics. Availability and lead time are confirmed per order.

What is PHENOBARBITAL SODIUM INJECTION, USP used for?

Control of generalized tonic-clonic and complex partial seizures; management of status epilepticus or acute seizure episodes.

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

Product details and regulatory record

DIN02304090
Brand namePHENOBARBITAL SODIUM INJECTION, USP
Generic / active ingredientPHENOBARBITAL SODIUM : 120 MG
ManufacturerSANDOZ CANADA INCORPORATED
Strength120 MG
Dosage formSOLUTION
Route of administrationINTRAMUSCULAR ; INTRAVENOUS
ScheduleCONTROLLED DRUGS (CDSA IV)
ATC codeN03AA02 PHENOBARBITAL
AHFS class28:12.04 ; 28:24.04
BiosimilarNo
Health Canada statusMARKETED
Status date29-Feb-2008
Original market date2008-02-29 00:00:00

How is it administered?

Deep IM or slow IV injection. Adults: 100-320 mg IV for anticonvulsant; 20 mg/kg IV for status epilepticus. Max 2 g daily. Slow administration is essential to prevent cardiovascular collapse.

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

How is it stored and handled?

Store between 15°C and 25°C. Protect from freezing. Protect from light. Do not use if precipitate present.

How is it supplied?

Boxes of 10 ampoules of 1 mL each.

Contraindications

Hypersensitivity to barbiturates; porphyria; severe respiratory depression; renal/hepatic impairment; sleep apnea; suicidal potential; alcoholism; drug dependence; uncontrolled pain; newborns.

Warnings and precautions

Potential for psychological/physiologic dependence. Risk of suicidal ideation. Serious skin reactions (SJS/TEN). Avoid rapid IV injection (risk of apnea/collapse). Risk of decreased bone density.

What can be used instead?

Other Canadian products sharing ATC code N03AA02 PHENOBARBITAL. 11 of 30 DINs in this group are currently marketed — marketed products are listed first, because that is what can actually be bought. These tables describe supply, not clinical equivalence: substitution rests with the prescriber or pharmacist, and interchangeability is determined provincially.

ProductStrengthFormManufacturerHealth Canada statusDIN
JAMP PHENOBARBITAL100 MGTABLETJAMP PHARMA CORPORATIONMARKETEDDIN 02557819
JAMP PHENOBARBITAL15 MGTABLETJAMP PHARMA CORPORATIONMARKETEDDIN 02557789
JAMP PHENOBARBITAL30 MGTABLETJAMP PHARMA CORPORATIONMARKETEDDIN 02557797
JAMP PHENOBARBITAL60 MGTABLETJAMP PHARMA CORPORATIONMARKETEDDIN 02557800
PHENOBARB100 MGTABLETPENDOPHARM DIVISION OF PHARMASCIENCE INCMARKETEDDIN 00178829
PHENOBARB15 MGTABLETPENDOPHARM DIVISION OF PHARMASCIENCE INCMARKETEDDIN 00178799
PHENOBARB30 MGTABLETPENDOPHARM DIVISION OF PHARMASCIENCE INCMARKETEDDIN 00178802
PHENOBARB60 MGTABLETPENDOPHARM DIVISION OF PHARMASCIENCE INCMARKETEDDIN 00178810
PHENOBARB ELIXIR5 MGSOLUTIONPENDOPHARM DIVISION OF PHARMASCIENCE INCMARKETEDDIN 00645575
PHENOBARBITAL SODIUM INJECTION, USP30 MGSOLUTIONSANDOZ CANADA INCORPORATEDMARKETEDDIN 02304082

Who else supplies PHENOBARBITAL worldwide?

Nexara tracks national medicine registries and published price lists across multiple markets. PHENOBARBITAL appears in 41 registered pack listings across 10 markets, published on 9 different national price bases. Where a Canadian route is closed, that is where an alternative route of supply starts — subject to the import rules in both countries.

Registered listings are not stock. Ask us to confirm what can actually be sourced for your order.

How can I get it?

Nexara Health supplies this product to licensed Canadian buyers — pharmacies, hospitals, clinics, licensed distributors, and clinical trial sponsors or their CROs. We confirm stock, pack size, expiry and pricing at the time of quotation. If the product is on backorder or in shortage, we identify equivalent alternatives and import options where permitted.

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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.

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.

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.

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Health Canada Drug Product Database (DPD), DIN 02304090. Last reviewed 2026-09-08. Nexara Health is a licensed wholesaler and supplies licensed entities only; consumer orders are routed to a partner pharmacy.