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01 4ATORVASTATIN CALCIUM
02 1Alendronic Acid
03 1Alfuzosin Hydrochloride
04 4Amlodipine Maleate
05 3CABOZANTINIB
06 1CETRORELIX ACETATE
07 1Cabergoline
08 1Carvedilol
09 2Citalopram Hydrobromide
10 1Clopidogrel
11 1DALBAVANCIN HYDROCHLORIDE
12 1ELAGOLIX
13 4ELTROMBOPAG CHOLINE
14 1Finasteride
15 1HYDROCORTISONE
16 2Lithium Carbonate
17 1MESALAMINE
18 1Meclozine Hydrochloride
19 2Montelukast Sodium
20 1PACLITAXEL
21 1PAZOPANIB HYDROCHLORIDE
22 2PRUCALOPRIDE
23 4Quinapril Hydrochloride
24 2Roxitromycin
25 1TADALAFIL
26 2THEOPHYLLINE
27 2TIOPRONIN
28 1Tamsulosin Hydrochloride
29 2VALBENAZINE TOSYLATE
30 4Venlafaxinhydroklorid
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01 1BAKER NORTON
02 20Ct Arzneimittel Gmbh
03 6Specifar S.A.
04 2TEVA
05 26TEVA PHARMS INC
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01 2CAPSULE;ORAL
02 2Chewable Tablet
03 12Film Coated Tablet
04 1LOTION;TOPICAL
05 1Lithium Carbonate 150Mg 50 Combined Oral Use
06 1Lithium Carbonate 300Mg 50 Combined Oral Use
07 2POWDER;INTRAVENOUS
08 1POWDER;SUBCUTANEOUS
09 1Prolonged-Release Hard Capsule
10 1Prolonged-Release Tablet
11 3TABLET, DELAYED RELEASE;ORAL
12 2TABLET, EXTENDED RELEASE;ORAL
13 1TABLET; FILM COATED
14 15TABLET;ORAL
15 10Tablet
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01 10.4MG
02 11%
03 1100MG
04 1100MG/VIAL
05 110MG
06 310mg
07 2150mg
08 11MG
09 1200MG
10 220MG
11 220mg
12 1225mg
13 12MG
14 13.125mg
15 2300MG
16 1300mg
17 130MG
18 137.5mg
19 240MG
20 240mg
21 1450MG
22 24mg
23 150 cps 150 mg
24 150 cps 300 mg
25 15MG
26 45mg
27 160MG
28 170MG
29 175MG
30 175mg
31 1800MG
32 180MG
33 1EQ 0.25MG BASE/VIAL
34 1EQ 10MG BASE
35 1EQ 18MG BASE
36 1EQ 200MG BASE
37 1EQ 20MG BASE
38 1EQ 36MG BASE
39 1EQ 40MG BASE
40 1EQ 500MG BASE/VIAL
41 1EQ 54MG BASE
42 1EQ 80MG BASE
43 1EQ 9MG BASE
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01 2Israel
02 6Malta
03 20Sweden
04 27USA
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Regulatory Info : Withdrawn
Registration Country : Malta
Dosage Form : Film Coated Tablet
Brand Name : Drofaz
Dosage Strength : 70MG
Packaging :
Approval Date : 2010-09-22
Application Number :
Regulatory Info : Withdrawn
Registration Country : Malta

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Regulatory Info : Withdrawn
Registration Country : Malta
Dosage Form : Prolonged-Release Tablet
Brand Name : Ofuxal
Dosage Strength : 10MG
Packaging :
Approval Date : 2010-11-05
Application Number :
Regulatory Info : Withdrawn
Registration Country : Malta

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Regulatory Info : Deregistered
Registration Country : Sweden
Dosage Form : Tablet
Brand Name : Amlopin
Dosage Strength : 10mg
Packaging :
Approval Date : 27/06/2003
Application Number : 20030627000132
Regulatory Info : Deregistered
Registration Country : Sweden

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Regulatory Info : Deregistered
Registration Country : Sweden
Dosage Form : Tablet
Brand Name : Amlopin
Dosage Strength : 5mg
Packaging :
Approval Date : 27/06/2003
Application Number : 20030627000125
Regulatory Info : Deregistered
Registration Country : Sweden

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Regulatory Info : Deregistered
Registration Country : Sweden
Dosage Form : Tablet
Brand Name : Pidolma
Dosage Strength : 10mg
Packaging :
Approval Date : 21/02/2003
Application Number : 20030221000118
Regulatory Info : Deregistered
Registration Country : Sweden

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Regulatory Info : Deregistered
Registration Country : Sweden
Dosage Form : Tablet
Brand Name : Pidolma
Dosage Strength : 5mg
Packaging :
Approval Date : 21/02/2003
Application Number : 20030221000101
Regulatory Info : Deregistered
Registration Country : Sweden

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Regulatory Info : RX
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : ATORVASTATIN CALCIUM
Dosage Strength : EQ 10MG BASE
Packaging :
Approval Date : 2025-11-13
Application Number : 220276
Regulatory Info : RX
Registration Country : USA

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Regulatory Info : RX
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : ATORVASTATIN CALCIUM
Dosage Strength : EQ 20MG BASE
Packaging :
Approval Date : 2025-11-13
Application Number : 220276
Regulatory Info : RX
Registration Country : USA

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Regulatory Info : RX
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : ATORVASTATIN CALCIUM
Dosage Strength : EQ 40MG BASE
Packaging :
Approval Date : 2025-11-13
Application Number : 220276
Regulatory Info : RX
Registration Country : USA

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Regulatory Info : RX
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : ATORVASTATIN CALCIUM
Dosage Strength : EQ 80MG BASE
Packaging :
Approval Date : 2025-11-13
Application Number : 220276
Regulatory Info : RX
Registration Country : USA

Assia Chemical Industries Ltd is a supplier offers 72 products (APIs, Excipients or Intermediates).
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