01 5Acetaminophen/Paracetamol
02 1Amantadine Hydrochloride
03 2Ambroxol
04 2Ambroxol Hydrochloride
05 1Ascorbic Acid
06 2Bromhexine
07 1Carbocisteine
08 4Clotrimazole
09 1Desloratadine
10 1Dextromethorphan
11 1Dextromethorphan Hydrobromide
12 2Diclofenac
13 2Etofenamate
14 1Fentanyl Citrate
15 1Flubendazole
16 1Furosemid
17 3Glycerol
18 2Hedera helix
19 1Hydrocortisone
20 4Ibuprofen
21 1Iron; Thiamine; Riboflavin; Niacin; Pyridoxine; Vitamin B 12; Folic Acid
22 1Isosorbide Dinitrate
23 1Lactulose
24 1Methyl Salicylate
25 1Metoclopramide
26 1Metronidazole
27 2N-Acetyl-L-Cysteine
28 2Paracetamol
29 1S-Carboxymethyl-L-Cysteine
30 1Sodium Chloride
31 1Thiamine; Riboflavin; Niacin; Pantothenic Acid; Pyridoxine; Vitamin B 12; Biotin; Folic Acid
32 1Vitamin A; Ascorbic Acid; Ergocalciferol; Vitamin E; Thiamine; Riboflavin; Niacin; Pyridoxine; Vitamin B 12; Folic Acid
01 2Laboratorios Basi - Industria Farmaceutica S.A.
02 40Laboratórios Basi
03 7Laboratórios Basi - Indústria Farmacêutica, S.A.
04 3Laboratórios Basi – Indústria Farmacêutica, S.A.
01 1Capsule
02 2Cream
03 1Cutaneous Solution
04 4Gel
05 1Injectable Solution
06 1Liquid Drops
07 4Liquid Solution
08 1Ointment
09 5Oral Solution
10 5Oral Suspension
11 1Ovule
12 1Solution For Infusion
13 1Solution For Injection
14 1Solution For Injection/Infusion
15 9Suppository
16 12Syrup
17 2Vaginal Cream
01 10.5MG/1ML
02 10.6G
03 10.8MG/1ML
04 11.6MG/1ML
05 1100MG
06 1100MG/1G
07 1100ML
08 310MG/1G
09 110MG/1ML
10 110MG/G
11 110mg/ml
12 1125MG
13 1150MG
14 11G
15 11MG/1ML
16 11MG/ML
17 120MG/1G
18 320MG/1ML
19 124MG/1ML
20 2250MG
21 12G
22 12MG/1ML
23 12MG/ML
24 130MG/1G
25 13MG/1ML
26 13MG/PUMP
27 340MG/1ML
28 2500MG
29 150MG/1G
30 150MG/1ML
31 150mcg/ml
32 15ML
33 161.1MG/1G
34 1667MG/1ML
35 16MG/1ML
36 16MG/ML
37 175MG
38 17MG/1ML
39 17mg/1mL
40 19MG/ML
41 4Blank
01 10Malta
02 40Portugal
03 2Sweden
Regulatory Info : EU CTD Dossier- Ready
Registration Country : Portugal
Dosage Form : Oral Suspension
Brand Name :
Dosage Strength : 40MG/1ML
Packaging : 1 Bottle- 85 ML
Approval Date :
Application Number :
Regulatory Info : EU CTD Dossier- Ready
Registration Country : Portugal
Regulatory Info : EU CTD Dossier- Ready
Registration Country : Portugal
Dosage Form : Oral Solution
Brand Name :
Dosage Strength : 24MG/1ML
Packaging : 1 Bottle- 100 ML, 200 ML
Approval Date :
Application Number :
Regulatory Info : EU CTD Dossier- Ready
Registration Country : Portugal
Regulatory Info : EU CTD Dossier- Ready
Registration Country : Portugal
Dosage Form : Suppository
Brand Name :
Dosage Strength : 125MG
Packaging : Strip- 10 or 12 Units
Approval Date :
Application Number :
Regulatory Info : EU CTD Dossier- Ready
Registration Country : Portugal
Regulatory Info : EU CTD Dossier- Ready
Registration Country : Portugal
Dosage Form : Suppository
Brand Name :
Dosage Strength : 250MG
Packaging : Strip- 10 or 12 Units
Approval Date :
Application Number :
Regulatory Info : EU CTD Dossier- Ready
Registration Country : Portugal
Regulatory Info : EU CTD Dossier- Ready
Registration Country : Portugal
Dosage Form : Suppository
Brand Name :
Dosage Strength : 500MG
Packaging : Strip- 10 or 12 Units
Approval Date :
Application Number :
Regulatory Info : EU CTD Dossier- Ready
Registration Country : Portugal
Regulatory Info : Authorised
Registration Country : Malta
Dosage Form : Capsule
Brand Name : Parkadina
Dosage Strength : 100MG
Packaging :
Approval Date : 2025-01-21
Application Number :
Regulatory Info : Authorised
Registration Country : Malta
Regulatory Info : EU CTD Dossier- 2 Sem 2017
Registration Country : Portugal
Dosage Form : Syrup
Brand Name :
Dosage Strength : 6MG/1ML
Packaging : 1 Bottle- 125 ML, 250 ML
Approval Date :
Application Number :
Regulatory Info : EU CTD Dossier- 2 Sem 2017
Registration Country : Portugal
Regulatory Info : EU CTD Dossier- 2 Sem 2017
Registration Country : Portugal
Dosage Form : Syrup
Brand Name :
Dosage Strength : 3MG/1ML
Packaging : 1 Bottle- 200 ML
Approval Date :
Application Number :
Regulatory Info : EU CTD Dossier- 2 Sem 2017
Registration Country : Portugal
Regulatory Info : Authorised
Registration Country : Malta
Dosage Form : Syrup
Brand Name : Broncosil,
Dosage Strength : 3MG/PUMP
Packaging :
Approval Date : 2023-10-16
Application Number :
Regulatory Info : Authorised
Registration Country : Malta
Regulatory Info : Authorised
Registration Country : Malta
Dosage Form : Syrup
Brand Name : Broncosil
Dosage Strength : 6MG/ML
Packaging :
Approval Date : 2024-11-19
Application Number :
Regulatory Info : Authorised
Registration Country : Malta
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