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TEVA-CITALOPRAM 20 MG

CITALOPRAM (CITALOPRAM HYDROBROMIDE) : 20 MG · DIN 02293218 · TEVA CANADA LIMITED

Health Canada status: MARKETED

What is TEVA-CITALOPRAM?

TEVA-CITALOPRAM 20 MG contains CITALOPRAM (CITALOPRAM HYDROBROMIDE) : 20 MG. It is listed in the Health Canada Drug Product Database under DIN 02293218, held by TEVA CANADA LIMITED, supplied as TABLET for ORAL administration. Health Canada currently lists it as marketed, status dated 03-Nov-2010. 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 TEVA-CITALOPRAM used for?

Symptomatic relief of depressive illness in adults.

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

DIN02293218
Brand nameTEVA-CITALOPRAM
Generic / active ingredientCITALOPRAM (CITALOPRAM HYDROBROMIDE) : 20 MG
ManufacturerTEVA CANADA LIMITED
Strength20 MG
Dosage formTABLET
Route of administrationORAL
SchedulePrescription
ATC codeN06AB04 CITALOPRAM
AHFS class28:16.04.20
BiosimilarNo
Health Canada statusMARKETED
Status date03-Nov-2010
Original market date2007-09-19 00:00:00

How is it administered?

Administer once daily (morning or evening) with or without food. Usual dose: 20 mg/day. Maximum: 40 mg/day. Titrate at intervals of at least one week. Taper gradually to discontinue.

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

How is it stored and handled?

Store at 15-30°C. (Note: Standard Teva storage for these forms, though specific text was truncated, the monograph header implies standard conditions).

How is it supplied?

10 mg: Bottles of 100. 20 mg: Bottles of 100, 500; Blisters of 30. 40 mg: Bottles of 100; Blisters of 30.

Contraindications

Hypersensitivity; Concomitant use of MAOIs (including linezolid, methylene blue); Concomitant use of pimozide; Known QT interval prolongation or congenital long QT syndrome.

Warnings and precautions

Serious risk of self-harm and suicidal behavior. Dose-dependent QT prolongation and Torsades de Pointes. Risk of Serotonin Syndrome. Do not discontinue abruptly.

Is CITALOPRAM in shortage in Canada?

A Canadian shortage report is on file for this molecule: Resolved — reported by JAMP PHARMA CORPORATION, last seen 03 Aug 2026. A shortage on one presentation does not always affect every DIN of the molecule — the alternatives below list what else is marketed in Canada. Nexara can confirm current availability and identify substitutions or import options where permitted.

Check availability for TEVA-CITALOPRAM

What can be used instead?

Other Canadian products sharing ATC code N06AB04 CITALOPRAM. 55 of 149 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
AG-CITALOPRAM10 MGTABLETANGITA PHARMA INC.MARKETEDDIN 02374617
AG-CITALOPRAM20 MGTABLETANGITA PHARMA INC.MARKETEDDIN 02339390
AG-CITALOPRAM40 MGTABLETANGITA PHARMA INC.MARKETEDDIN 02339404
AG-CITALOPRAM TABLETS10 MGTABLETANGITA PHARMA INC.MARKETEDDIN 02513676
AG-CITALOPRAM TABLETS20 MGTABLETANGITA PHARMA INC.MARKETEDDIN 02513684
AG-CITALOPRAM TABLETS30 MGTABLETANGITA PHARMA INC.MARKETEDDIN 02543060
AG-CITALOPRAM TABLETS40 MGTABLETANGITA PHARMA INC.MARKETEDDIN 02513692
APO-CITALOPRAM20 MGTABLETAPOTEX INCMARKETEDDIN 02246056
APO-CITALOPRAM40 MGTABLETAPOTEX INCMARKETEDDIN 02246057
AURO-CITALOPRAM20 MGTABLETAURO PHARMA INCMARKETEDDIN 02275562

Who else supplies CITALOPRAM worldwide?

Nexara tracks national medicine registries and published price lists across multiple markets. CITALOPRAM appears in 433 registered pack listings across 15 markets, published on 13 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 02293218. Last reviewed 2026-09-08. Nexara Health is a licensed wholesaler and supplies licensed entities only; consumer orders are routed to a partner pharmacy.