Our Portfolio

export-table

Export table

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PRODUCT NAME

THERAPEUTIC AREA

PHARMACEUTICAL
FORM

STRENGTH

REFERENCE
PRODUCT

Antineoplastic & Immunomodulating Agents
Film-coated tablets
5 mg
10 mg
Xeljanz / Pfizer
Antineoplastic & Immunomodulating Agents
Prolonged-release tablet
11 mg
Xeljanz / Pfizer
Respiratory system
Inhalation powder
85/43 mcg
Ultibro Breezhaler / Novartis
Respiratory system
Inhalation powder
44 mcg
Seebri Breezhaler / Novartis
Nervous system
Powder and solvent for prolonged-release suspension for injection
300 mg
400 mg
Abilify Maintena/Otsuka
Alimentary tract & metabolism
Film-coated tablets
5mg/500mg
5mg/850mg
5mg/1000 mg
12.5mg/500mg
12.5mg/850mg
12.5mg/1000mg
Synjardy / Boehringer Ingelheim
Nervous system
Film-coated tablets
5 mg
10 mg
15 mg
20 mg
Brintellix / H. Lundbeck A/S
Alimentary tract & metabolism
Film-coated tablets
10 mg/5 mg
25 mg/5 mg
Glyxambi/ Boehringer Ingelheim
Antineoplastic & Immunomodulating Agents
Film-coated tablets
10 mg
20 mg
30 mg
Otezla / Celgene
Alimentary tract & metabolism
Film-coated tablets
2.5/500 mg
2.5/850 mg
2.5/1000 mg
Jentadueto / Boehringer Ingelheim
Cardiovascular System
Film-coated tablets
24mg / 26mg
49mg / 51mg
97mg / 103mg
Entresto / Novartis
* Polpharma Group API
(1) BEQ study against Canadian reference product available
(2) BEQ study against Canadian reference product on-going
(3) BEQ study against Canadian reference product planned
^ This product is not offered for sale or made available in Germany due to patent (SPC) protection.

DISCLAIMER
Products protected by patents (SPC) in Poland are developed solely for the purpose of Regulatory Submissions or R&D purposes intended to support Regulatory Submissions. These products are not offered for sale or made available in countries where such products are subject to patent (SPC) protection and where the offer for sale or any related activity constitutes patent infringement. It is within the buyer’s responsibility and liability to check the patent situation of the product in the import market(s).

Our Portfolio

Tofacitinib IR

THERAPEUTIC AREA

Antineoplastic & Immunomodulating Agents

PHARMACEUTICAL FORM

Film-coated tablets

REFERENCE PRODUCT

Xeljanz / Pfizer

STRENGTH

5 mg
 | 10 mg

DOSSIER AVAILABILITY

Early stage

Tofacitinib SR^

THERAPEUTIC AREA

Antineoplastic & Immunomodulating Agents

PHARMACEUTICAL FORM

Prolonged-release tablet

REFERENCE PRODUCT

Xeljanz / Pfizer

STRENGTH

11 mg

DOSSIER AVAILABILITY

Early stage

Indacaterol / Glycopyrronium^

THERAPEUTIC AREA

Respiratory system

PHARMACEUTICAL FORM

Inhalation powder

REFERENCE PRODUCT

Ultibro Breezhaler / Novartis

STRENGTH

85/43 mcg

DOSSIER AVAILABILITY

2026 Q2

Glycopyrronium^

THERAPEUTIC AREA

Respiratory system

PHARMACEUTICAL FORM

Inhalation powder

REFERENCE PRODUCT

Seebri Breezhaler / Novartis

STRENGTH

44 mcg

DOSSIER AVAILABILITY

2025 Q4

Aripiprazole*

THERAPEUTIC AREA

Nervous system

PHARMACEUTICAL FORM

Powder and solvent for prolonged-release suspension for injection

REFERENCE PRODUCT

Abilify Maintena/Otsuka

STRENGTH

300 mg
 | 400 mg

DOSSIER AVAILABILITY

2025 Q3

Empagliflozin* / Metformin^

THERAPEUTIC AREA

Alimentary tract & metabolism

PHARMACEUTICAL FORM

Film-coated tablets

REFERENCE PRODUCT

Synjardy / Boehringer Ingelheim

STRENGTH

5mg/500mg
 |  5mg/850mg
 | 5mg/1000 mg
 | 12.5mg/500mg
 | 12.5mg/850mg
 | 12.5mg/1000mg

DOSSIER AVAILABILITY

2025 Q2

* Polpharma Group API

(1) BEQ study against Canadian reference product available
(2) BEQ study against Canadian reference product on-going
(3) BEQ study against Canadian reference product planned
^ This product is not offered for sale or made available in Germany due to patent (SPC) protection.

DISCLAIMER
Products protected by patents (SPC) in Poland are developed solely for the purpose of Regulatory Submissions or R&D purposes intended to support Regulatory Submissions. These products are not offered for sale or made available in countries where such products are subject to patent (SPC) protection and where the offer for sale or any related activity constitutes patent infringement. It is within the buyer’s responsibility and liability to check the patent situation of the product in the import market(s).