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Approved Drug Products containing Metformin Hydrochloride listed with Health Canada. Original Data : Health Canada Website

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METFORMIN HYDROCHLORIDE

Metformin Hydrochloride

SITAGLIPTIN (SITAGLIPTIN PHOSPHATE MONOHYDRATE)

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TABLET

TABLET (EXTENDED-RELEASE)

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ACT METFORMIN

APO-METFORMIN - TAB 500MG

APO-METFORMIN 850 MG TABLETS

APO-METFORMIN ER

AURO-METFORMIN

DOM-METFORMIN

GLUCOPHAGE

GLUMETZA

INVOKAMET

JAMP-METFORMIN

JANUMET

JANUMET XR

JANUVIA

JENTADUETO

KAZANO

KOMBOGLYZE

METFORMIN

METFORMIN FC

MINT-METFORMIN

PMS-METFORMIN

PMS-METFORMIN - TAB 500MG

PRO-METFORMIN

RAN-METFORMIN

RATIO-METFORMIN

RIVA-METFORMIN

SANDOZ METFORMIN FC

SEGLUROMET

SEPTA-METFORMIN

SYNJARDY

XIGDUO

Dosage Form

TABLET

Dosage Strength

850MG

Approval Date

Brand Name

GLUCOPHAGE

Application Number

2162849

Packaging Presentation

100

Regulatory Information

Prescription

Supporting Information

Dosage Form

TABLET

Dosage Strength

500MG

Approval Date

Brand Name

GLUCOPHAGE

Application Number

2099233

Packaging Presentation

100/500

Regulatory Information

Prescription

Supporting Information

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Dosage Form

TABLET (EXTENDED-RELEASE)

Dosage Strength

500MG

Approval Date

Brand Name

APO-METFORMIN ER

Application Number

2305062

Packaging Presentation

Regulatory Information

Prescription

Supporting Information

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Dosage Form

TABLET (EXTENDED-RELEASE)

Dosage Strength

1000MG

Approval Date

Brand Name

APO-METFORMIN ER

Application Number

2460653

Packaging Presentation

100/500

Regulatory Information

Prescription

Supporting Information

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Dosage Form

TABLET

Dosage Strength

500MG

Approval Date

Brand Name

APO-METFORMIN - TAB 500MG

Application Number

2167786

Packaging Presentation

100,500 TABLETS

Regulatory Information

Prescription

Supporting Information

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Dosage Form

TABLET

Dosage Strength

850MG

Approval Date

Brand Name

APO-METFORMIN 850 MG TABLETS

Application Number

2229785

Packaging Presentation

100

Regulatory Information

Prescription

Supporting Information

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Dosage Form

TABLET

Dosage Strength

500MG

Approval Date

Brand Name

KOMBOGLYZE

Application Number

2389169

Packaging Presentation

60

Regulatory Information

Prescription

Supporting Information

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Dosage Form

TABLET

Dosage Strength

850MG

Approval Date

Brand Name

KOMBOGLYZE

Application Number

2389177

Packaging Presentation

60

Regulatory Information

Prescription

Supporting Information

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Dosage Form

TABLET

Dosage Strength

1000MG

Approval Date

Brand Name

KOMBOGLYZE

Application Number

2389185

Packaging Presentation

60

Regulatory Information

Prescription

Supporting Information

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Dosage Form

TABLET

Dosage Strength

850MG

Approval Date

Brand Name

XIGDUO

Application Number

2449935

Packaging Presentation

14/60

Regulatory Information

Prescription

Supporting Information

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Dosage Form

TABLET

Dosage Strength

1000MG

Approval Date

Brand Name

XIGDUO

Application Number

2449943

Packaging Presentation

14/60

Regulatory Information

Prescription

Supporting Information

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Dosage Form

TABLET

Dosage Strength

500MG

Approval Date

Brand Name

AURO-METFORMIN

Application Number

2438275

Packaging Presentation

100/500

Regulatory Information

Prescription

Supporting Information

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Dosage Form

TABLET

Dosage Strength

850MG

Approval Date

Brand Name

AURO-METFORMIN

Application Number

2438283

Packaging Presentation

100/360/500

Regulatory Information

Prescription

Supporting Information

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Dosage Form

TABLET

Dosage Strength

500MG

Approval Date

Brand Name

JENTADUETO

Application Number

2403250

Packaging Presentation

14/60

Regulatory Information

Prescription

Supporting Information

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Dosage Form

TABLET

Dosage Strength

850MG

Approval Date

Brand Name

JENTADUETO

Application Number

2403269

Packaging Presentation

14/60

Regulatory Information

Prescription

Supporting Information

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Dosage Form

TABLET

Dosage Strength

1000MG

Approval Date

Brand Name

JENTADUETO

Application Number

2403277

Packaging Presentation

14/60

Regulatory Information

Prescription

Supporting Information

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Dosage Form

TABLET

Dosage Strength

500MG

Approval Date

Brand Name

SYNJARDY

Application Number

2456575

Packaging Presentation

10/60

Regulatory Information

Prescription

Supporting Information

Request an Update of Your Company Information, Events & Sales Content

Dosage Form

TABLET

Dosage Strength

850MG

Approval Date

Brand Name

SYNJARDY

Application Number

2456583

Packaging Presentation

10/60

Regulatory Information

Prescription

Supporting Information

Request an Update of Your Company Information, Events & Sales Content

Dosage Form

TABLET

Dosage Strength

1000MG

Approval Date

Brand Name

SYNJARDY

Application Number

2456591

Packaging Presentation

10/60

Regulatory Information

Prescription

Supporting Information

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Dosage Form

TABLET

Dosage Strength

500MG

Approval Date

Brand Name

SYNJARDY

Application Number

2456605

Packaging Presentation

10/60

Regulatory Information

Prescription

Supporting Information

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Dosage Form

TABLET

Dosage Strength

850MG

Approval Date

Brand Name

SYNJARDY

Application Number

2456613

Packaging Presentation

10/60

Regulatory Information

Prescription

Supporting Information

Request an Update of Your Company Information, Events & Sales Content

Dosage Form

TABLET

Dosage Strength

1000MG

Approval Date

Brand Name

SYNJARDY

Application Number

2456621

Packaging Presentation

10/60

Regulatory Information

Prescription

Supporting Information

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Dosage Form

TABLET

Dosage Strength

1000MG

Approval Date

Brand Name

INVOKAMET

Application Number

2455420

Packaging Presentation

60

Regulatory Information

Prescription

Supporting Information

Request an Update of Your Company Information, Events & Sales Content

Dosage Form

TABLET

Dosage Strength

500MG

Approval Date

Brand Name

INVOKAMET

Application Number

2455404

Packaging Presentation

60

Regulatory Information

Prescription

Supporting Information

Request an Update of Your Company Information, Events & Sales Content

Dosage Form

TABLET

Dosage Strength

850MG

Approval Date

Brand Name

INVOKAMET

Application Number

2455412

Packaging Presentation

60

Regulatory Information

Prescription

Supporting Information

Request an Update of Your Company Information, Events & Sales Content

Dosage Form

TABLET

Dosage Strength

500MG

Approval Date

Brand Name

INVOKAMET

Application Number

2455439

Packaging Presentation

60

Regulatory Information

Prescription

Supporting Information

Request an Update of Your Company Information, Events & Sales Content

Dosage Form

TABLET

Dosage Strength

850MG

Approval Date

Brand Name

INVOKAMET

Application Number

2455447

Packaging Presentation

60

Regulatory Information

Prescription

Supporting Information

Request an Update of Your Company Information, Events & Sales Content

Dosage Form

TABLET

Dosage Strength

1000MG

Approval Date

Brand Name

INVOKAMET

Application Number

2455455

Packaging Presentation

60

Regulatory Information

Prescription

Supporting Information

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Dosage Form

TABLET

Dosage Strength

500MG

Approval Date

Brand Name

DOM-METFORMIN

Application Number

2229994

Packaging Presentation

100

Regulatory Information

Prescription

Supporting Information

Request an Update of Your Company Information, Events & Sales Content

Dosage Form

TABLET

Dosage Strength

850MG

Approval Date

Brand Name

DOM-METFORMIN

Application Number

2242726

Packaging Presentation

100

Regulatory Information

Prescription

Supporting Information

Request an Update of Your Company Information, Events & Sales Content

Dosage Form

TABLET

Dosage Strength

500MG

Approval Date

Brand Name

JAMP-METFORMIN

Application Number

2380196

Packaging Presentation

100/500

Regulatory Information

Prescription

Supporting Information

Request an Update of Your Company Information, Events & Sales Content

Dosage Form

TABLET

Dosage Strength

850MG

Approval Date

Brand Name

JAMP-METFORMIN

Application Number

2380218

Packaging Presentation

100/500

Regulatory Information

Prescription

Supporting Information

Request an Update of Your Company Information, Events & Sales Content

Dosage Form

TABLET

Dosage Strength

500MG

Approval Date

Brand Name

RIVA-METFORMIN

Application Number

2239081

Packaging Presentation

100/500

Regulatory Information

Prescription

Supporting Information

Request an Update of Your Company Information, Events & Sales Content

Dosage Form

TABLET

Dosage Strength

850MG

Approval Date

Brand Name

RIVA-METFORMIN

Application Number

2242783

Packaging Presentation

100/500

Regulatory Information

Prescription

Supporting Information

Request an Update of Your Company Information, Events & Sales Content

Dosage Form

TABLET

Dosage Strength

500MG

Approval Date

Brand Name

JANUMET

Application Number

2333856

Packaging Presentation

60

Regulatory Information

Prescription

Supporting Information

Request an Update of Your Company Information, Events & Sales Content

Dosage Form

TABLET

Dosage Strength

850MG

Approval Date

Brand Name

JANUMET

Application Number

2333864

Packaging Presentation

60

Regulatory Information

Prescription

Supporting Information

Request an Update of Your Company Information, Events & Sales Content

Dosage Form

TABLET

Dosage Strength

1000MG

Approval Date

Brand Name

JANUMET

Application Number

2333872

Packaging Presentation

60

Regulatory Information

Prescription

Supporting Information

Request an Update of Your Company Information, Events & Sales Content

Dosage Form

TABLET (EXTENDED-RELEASE)

Dosage Strength

500MG

Approval Date

Brand Name

JANUMET XR

Application Number

2416786

Packaging Presentation

60

Regulatory Information

Prescription

Supporting Information

Request an Update of Your Company Information, Events & Sales Content

Dosage Form

TABLET (EXTENDED-RELEASE)

Dosage Strength

1000MG

Approval Date

Brand Name

JANUMET XR

Application Number

2416794

Packaging Presentation

60

Regulatory Information

Prescription

Supporting Information

Request an Update of Your Company Information, Events & Sales Content

Dosage Form

TABLET (EXTENDED-RELEASE)

Dosage Strength

1000MG

Approval Date

Brand Name

JANUMET XR

Application Number

2416808

Packaging Presentation

30

Regulatory Information

Prescription

Supporting Information

Request an Update of Your Company Information, Events & Sales Content

Dosage Form

TABLET

Dosage Strength

500MG

Approval Date

Brand Name

SEGLUROMET

Application Number

2476215

Packaging Presentation

60

Regulatory Information

Prescription

Supporting Information

Request an Update of Your Company Information, Events & Sales Content

Dosage Form

TABLET

Dosage Strength

1000MG

Approval Date

Brand Name

SEGLUROMET

Application Number

2476223

Packaging Presentation

60

Regulatory Information

Prescription

Supporting Information

Request an Update of Your Company Information, Events & Sales Content

Dosage Form

TABLET

Dosage Strength

500MG

Approval Date

Brand Name

SEGLUROMET

Application Number

2476231

Packaging Presentation

60

Regulatory Information

Prescription

Supporting Information

Request an Update of Your Company Information, Events & Sales Content

Dosage Form

TABLET

Dosage Strength

1000MG

Approval Date

Brand Name

SEGLUROMET

Application Number

2476258

Packaging Presentation

60

Regulatory Information

Prescription

Supporting Information

Request an Update of Your Company Information, Events & Sales Content

Dosage Form

TABLET

Dosage Strength

100MG

Approval Date

Brand Name

JANUVIA

Application Number

2303922

Packaging Presentation

30/100

Regulatory Information

Prescription

Supporting Information

Request an Update of Your Company Information, Events & Sales Content

Dosage Form

TABLET

Dosage Strength

50MG

Approval Date

Brand Name

JANUMET

Application Number

2333856

Packaging Presentation

60

Regulatory Information

Prescription

Supporting Information

Request an Update of Your Company Information, Events & Sales Content

Dosage Form

TABLET

Dosage Strength

50MG

Approval Date

Brand Name

JANUMET

Application Number

2333872

Packaging Presentation

60

Regulatory Information

Prescription

Supporting Information

Request an Update of Your Company Information, Events & Sales Content

Dosage Form

TABLET

Dosage Strength

50MG

Approval Date

Brand Name

JANUMET

Application Number

2333864

Packaging Presentation

60

Regulatory Information

Prescription

Supporting Information

Request an Update of Your Company Information, Events & Sales Content

Dosage Form

TABLET

Dosage Strength

25MG

Approval Date

Brand Name

JANUVIA

Application Number

2388839

Packaging Presentation

12

Regulatory Information

Prescription

Supporting Information

Request an Update of Your Company Information, Events & Sales Content

Dosage Form

TABLET

Dosage Strength

50MG

Approval Date

Brand Name

JANUVIA

Application Number

2388847

Packaging Presentation

12

Regulatory Information

Prescription

Supporting Information

Request an Update of Your Company Information, Events & Sales Content

Dosage Form

TABLET (EXTENDED-RELEASE)

Dosage Strength

50MG

Approval Date

Brand Name

JANUMET XR

Application Number

2416786

Packaging Presentation

60

Regulatory Information

Prescription

Supporting Information

Request an Update of Your Company Information, Events & Sales Content

Dosage Form

TABLET (EXTENDED-RELEASE)

Dosage Strength

50MG

Approval Date

Brand Name

JANUMET XR

Application Number

2416794

Packaging Presentation

60

Regulatory Information

Prescription

Supporting Information

Request an Update of Your Company Information, Events & Sales Content

Dosage Form

TABLET (EXTENDED-RELEASE)

Dosage Strength

100MG

Approval Date

Brand Name

JANUMET XR

Application Number

2416808

Packaging Presentation

30

Regulatory Information

Prescription

Supporting Information

Request an Update of Your Company Information, Events & Sales Content

Dosage Form

TABLET

Dosage Strength

500MG

Approval Date

Brand Name

MINT-METFORMIN

Application Number

2388766

Packaging Presentation

100/500

Regulatory Information

Prescription

Supporting Information

Request an Update of Your Company Information, Events & Sales Content

Dosage Form

TABLET

Dosage Strength

850MG

Approval Date

Brand Name

MINT-METFORMIN

Application Number

2388774

Packaging Presentation

100/500

Regulatory Information

Prescription

Supporting Information

Request an Update of Your Company Information, Events & Sales Content

Dosage Form

TABLET

Dosage Strength

500MG

Approval Date

Brand Name

PMS-METFORMIN - TAB 500MG

Application Number

Packaging Presentation

100/500

Regulatory Information

Prescription

Supporting Information

Request an Update of Your Company Information, Events & Sales Content

Dosage Form

TABLET

Dosage Strength

850MG

Approval Date

Brand Name

PMS-METFORMIN

Application Number

Packaging Presentation

100

Regulatory Information

Prescription

Supporting Information

Request an Update of Your Company Information, Events & Sales Content

Dosage Form

TABLET

Dosage Strength

500MG

Approval Date

Brand Name

PMS-METFORMIN - TAB 500MG

Application Number

2223562

Packaging Presentation

100/500

Regulatory Information

Prescription

Supporting Information

Request an Update of Your Company Information, Events & Sales Content

Dosage Form

TABLET

Dosage Strength

850MG

Approval Date

Brand Name

PMS-METFORMIN

Application Number

2242589

Packaging Presentation

100

Regulatory Information

Prescription

Supporting Information

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Dosage Form

TABLET

Dosage Strength

850MG

Approval Date

Brand Name

PRO-METFORMIN

Application Number

2314894

Packaging Presentation

100/500

Regulatory Information

Prescription

Supporting Information

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Dosage Form

TABLET

Dosage Strength

500MG

Approval Date

Brand Name

PRO-METFORMIN

Application Number

2314908

Packaging Presentation

100/500

Regulatory Information

Prescription

Supporting Information

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Dosage Form

TABLET

Dosage Strength

500MG

Approval Date

Brand Name

RAN-METFORMIN

Application Number

2269031

Packaging Presentation

100/300/500

Regulatory Information

Prescription

Supporting Information

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Dosage Form

TABLET

Dosage Strength

850MG

Approval Date

Brand Name

RAN-METFORMIN

Application Number

2269058

Packaging Presentation

100/360/500

Regulatory Information

Prescription

Supporting Information

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Dosage Form

TABLET

Dosage Strength

500MG

Approval Date

Brand Name

SANDOZ METFORMIN FC

Application Number

2246820

Packaging Presentation

100/500

Regulatory Information

Prescription

Supporting Information

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Dosage Form

TABLET

Dosage Strength

850MG

Approval Date

Brand Name

SANDOZ METFORMIN FC

Application Number

2246821

Packaging Presentation

100/500

Regulatory Information

Prescription

Supporting Information

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Dosage Form

TABLET

Dosage Strength

500MG

Approval Date

Brand Name

METFORMIN

Application Number

2353377

Packaging Presentation

100/500

Regulatory Information

Prescription

Supporting Information

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Dosage Form

TABLET

Dosage Strength

850MG

Approval Date

Brand Name

METFORMIN

Application Number

2353385

Packaging Presentation

100/500

Regulatory Information

Prescription

Supporting Information

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Dosage Form

TABLET

Dosage Strength

500MG

Approval Date

Brand Name

SEPTA-METFORMIN

Application Number

2379767

Packaging Presentation

100/500

Regulatory Information

Prescription

Supporting Information

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Dosage Form

TABLET

Dosage Strength

850MG

Approval Date

Brand Name

SEPTA-METFORMIN

Application Number

2379775

Packaging Presentation

100

Regulatory Information

Prescription

Supporting Information

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Dosage Form

TABLET

Dosage Strength

500MG

Approval Date

Brand Name

METFORMIN FC

Application Number

2385341

Packaging Presentation

100/360/500

Regulatory Information

Prescription

Supporting Information

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Dosage Form

TABLET

Dosage Strength

850MG

Approval Date

Brand Name

METFORMIN FC

Application Number

2385368

Packaging Presentation

100/500

Regulatory Information

Prescription

Supporting Information

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Dosage Form

TABLET

Dosage Strength

500MG

Approval Date

Brand Name

KAZANO

Application Number

2417219

Packaging Presentation

60

Regulatory Information

Prescription

Supporting Information

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Dosage Form

TABLET

Dosage Strength

850MG

Approval Date

Brand Name

KAZANO

Application Number

2417227

Packaging Presentation

60

Regulatory Information

Prescription

Supporting Information

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Dosage Form

TABLET

Dosage Strength

1000MG

Approval Date

Brand Name

KAZANO

Application Number

2417235

Packaging Presentation

60

Regulatory Information

Prescription

Supporting Information

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Dosage Form

TABLET

Dosage Strength

850MG

Approval Date

Brand Name

RATIO-METFORMIN

Application Number

2242931

Packaging Presentation

100/500

Regulatory Information

Prescription

Supporting Information

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Dosage Form

TABLET

Dosage Strength

500MG

Approval Date

Brand Name

RATIO-METFORMIN

Application Number

2242974

Packaging Presentation

100/500

Regulatory Information

Prescription

Supporting Information

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Dosage Form

TABLET

Dosage Strength

500MG

Approval Date

Brand Name

ACT METFORMIN

Application Number

2257726

Packaging Presentation

100/500

Regulatory Information

Prescription

Supporting Information

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Dosage Form

TABLET

Dosage Strength

850MG

Approval Date

Brand Name

ACT METFORMIN

Application Number

2257734

Packaging Presentation

100/500

Regulatory Information

Prescription

Supporting Information

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Dosage Form

TABLET (EXTENDED-RELEASE)

Dosage Strength

1000MG

Approval Date

Brand Name

GLUMETZA

Application Number

2300451

Packaging Presentation

7/90

Regulatory Information

Prescription

Supporting Information

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Dosage Form

TABLET (EXTENDED-RELEASE)

Dosage Strength

500MG

Approval Date

Brand Name

GLUMETZA

Application Number

2268493

Packaging Presentation

500

Regulatory Information

Prescription

Supporting Information

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