ATROVENT NASAL SPRAY 21 MCG — DIN 02163705
IPRATROPIUM BROMIDE : 21 MCG · SANOFI-AVENTIS CANADA INC · SOLUTION · wholesale supply in Canada
Health Canada status: CANCELLED POST MARKET
What is ATROVENT NASAL SPRAY?
ATROVENT NASAL SPRAY 21 MCG contains IPRATROPIUM BROMIDE : 21 MCG. It is listed in the Health Canada Drug Product Database under DIN 02163705, held by SANOFI-AVENTIS CANADA INC, supplied as SOLUTION for NASAL administration. Health Canada currently lists it as cancelled post market, status dated 13-Nov-2018. 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 ATROVENT NASAL SPRAY used for?
ATROVENT (ipratropium bromide) Nasal Spray 0.03% is indicated for: treatment of symptomatic relief of rhinorrhea associated with allergic or non-allergic perennial rhinitis. ATROVENT (ipratropium bromide) Nasal Spray 0.06% is indicated for: treatment of symptomatic relief of rhinorrhea associated with the common cold.
Authorized indication as written in the Health Canada product monograph. For healthcare professionals and licensed purchasers; this is not medical advice.
How much does Ipratropium Bromide cost around the world?
Ipratropium Bromide is listed on 2 of the national price registers Nexara ingests. Each country publishes on a different basis, so those figures are not comparable with one another — or with a Canadian wholesale price.
What a market publishes matters more than the number it publishes. Austria publishes a KVP (Kassenverkaufspreis); Norway publishes a max AUP (pharmacy retail). Comparing an ex-factory ceiling against a pharmacy public price tells you nothing about either, and comparing either against a Canadian landed cost tells you less.
| Market | Price basis published there | Brands | Packs listed | Range |
|---|---|---|---|---|
| Norway | max AUP (pharmacy retail) | 1 | 5 | NOK███.██ |
| Austria | KVP (Kassenverkaufspreis) | 1 | 1 | EUR███.██ |
6 pack listings across 2 brand entries and 2 price bases, refreshed 07 Sep 2026. Ranges span every Ipratropium Bromide pack in that market, so a high figure is usually a larger pack rather than the same product.
This table is a regulatory record of where the molecule is listed. The DIN on this page is no longer authorized for sale in Canada, so Nexara does not quote it — see the alternatives above.
Is there a generic Ipratropium Bromide 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.
5 holders have a Canadian DIN containing Ipratropium Bromide, across 7 DINs, of which 1 are currently marketed. Marketed count is the number that matters: an approval that is not marketed cannot be bought.
| Market authorization holder | DINs | Marketed | Brand names | Position |
|---|---|---|---|---|
| AA PHARMA INC | 2 | 1 | IPRAVENT | Sourceable in Canada |
| SANOFI-AVENTIS CANADA INC | 2 | 0 | ATROVENT NASAL SPRAY | No marketed DIN |
| DOMINION PHARMACAL | 1 | 0 | DOM-IPRATROPIUM | No marketed DIN |
| PHARMEL INC | 1 | 0 | IPRATROPIUM | No marketed DIN |
| RATIOPHARM INC DIVISION OF TEVA CANADA LIMITED | 1 | 0 | RATIO-IPRATROPIUM | No 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 label | 21 MCG |
|---|---|
| Dosage form | SOLUTION |
| Route | NASAL |
| Pack configuration (monograph) | null |
| Storage | null |
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 substance | Ipratropium Bromide |
|---|---|
| ATC code | R01AX03 |
| AHFS class | 52:92.00 |
| Biosimilar biologic | No |
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) | 02163705 |
|---|---|
| DIN (unpadded, as printed on some documents) | 2163705 |
| Brand name | ATROVENT NASAL SPRAY |
| Generic / active ingredient | IPRATROPIUM BROMIDE : 21 MCG |
| Market authorization holder | SANOFI-AVENTIS CANADA INC |
| Health Canada schedule | Prescription |
| ATC code | R01AX03 |
| ATC anatomical main group | R — Respiratory system |
| ATC therapeutic subgroup | R01AX |
| Current status | CANCELLED POST MARKET |
| Status date | 13-Nov-2018 |
| Original market date | 1995-12-31 00:00:00 |
| Status source | Live Health Canada DPD sync |
Verify on the primary sources
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
1 of 7 Canadian DINs for this molecule are currently marketed. Marketed products are listed first.
| Product | Strength | Form | Holder | Health Canada status | DIN |
|---|---|---|---|---|---|
| IPRAVENT | 42 MCG | SOLUTION | AA PHARMA INC | MARKETED | 02246084 |
| ATROVENT NASAL SPRAY | 42 MCG | SOLUTION | SANOFI-AVENTIS CANADA INC | CANCELLED POST MARKET | 02163713 |
| DOM-IPRATROPIUM | 21 MCG | SOLUTION | DOMINION PHARMACAL | CANCELLED POST MARKET | 02240508 |
| IPRATROPIUM | 0.30 MG | LIQUID | PHARMEL INC | CANCELLED PRE MARKET | 02240474 |
| IPRAVENT | 21 MCG | SOLUTION | AA PHARMA INC | DORMANT | 02246083 |
| RATIO-IPRATROPIUM | 21 MCG | METERED-DOSE PUMP | RATIOPHARM INC DIVISION OF TEVA CANADA LIMITED | CANCELLED POST MARKET | 02240072 |
2 · Same class — other molecules in ATC R01AX
| Molecule | Canadian brands | DINs | Marketed | Sourceable |
|---|---|---|---|---|
| Various | AIRLIFE STERILE WATER FOR INHALATION USP · DEY-PAK SODIUM CHLORIDE SOLUTION 0.45% · DEY-PAK SODIUM CHLORIDE SOLUTION 10% · DEY-PAK SODIUM CHLORIDE SOLUTION 3% · +12 more | 17 | 3 | Yes |
| Ipratropium Bromide | ATROVENT NASAL SPRAY · DOM-IPRATROPIUM · IPRATROPIUM · IPRAVENT · +1 more | 7 | 1 | Yes |
| Combinations | AIRLIFE MODUDOSE 0.45% SODIUM CHLORIDE SOLUTION · AIRLIFE SODIUM CHLORIDE INHALATION SOLUTION USP (0.45%) · AIRLIFE SODIUM CHLORIDE INHALATION SOLUTION USP (0.9%) · BACTERIOSTATIC NACL DILUENT FOR INHALATION · +13 more | 18 | 0 | Not 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 R01A
| ATC subgroup | Molecules | DINs | Marketed |
|---|---|---|---|
| R01AD | Beclomethasone · Budesonide · Ciclesonide · Flunisolide · Fluticasone · +5 more | 55 | 24 |
| R01AA | Ephedrine · Oxymetazoline · Phenylephrine · Xylometazoline | 76 | 18 |
| R01AB | Ephedrine · Naphazoline · Oxymetazoline · Phenylephrine | 12 | 1 |
| R01AC | Cromoglicic Acid · Levocabastine | 6 | 0 |
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.
What else is ATROVENT NASAL SPRAY called?
The same molecule, Ipratropium Bromide, is registered under other names elsewhere. Buyers and prescribers searching from outside Canada — or working from a foreign prescription or tender document — often know it by one of these:
| Name | Script | Registered in |
|---|---|---|
| Atrovent | Latin | Norway |
Names are taken from national medicine registers and published price lists. A product registered abroad is not authorized for sale in Canada unless it holds its own DIN; import is possible only through the routes Health Canada permits.
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.