01 6Atenolol
02 4Atenolol; Chlorthalidone
03 8Calcitriol
04 2Catumaxomab
05 3Cladribine
06 4Clobazam
07 8Diazepam
08 3Famciclovir
09 4Granisetron
10 3Granisetron Hydrochloride
11 2Granisetrone
12 1Ibandronate sodium
13 5Ibandronate sodium monohydrate
14 6Ibandronic Acid
15 3Ibandronic acid
16 2KETOROLAC TROMETHAMINE
17 2Ketorolac
18 4Ketorolac Trometamol
19 1Ketorolaktrometamol
20 6Lisinopril
21 8Lisinopril dihydrate
22 1Lisinopril dihydrate; Hydrochlorothiazide
23 3Lisinopril; Hydrochlorothiazide
24 1Macimorelin Acetate
25 1Macimorelin acetate
26 1Macimoreline Acetate
27 6NAPROXEN
28 2NAPROXEN SODIUM
29 1Naproxen
30 1Naproxen Sodium
31 2Olsalazine Sodium
32 2Olsalazine sodium
33 1Prochlorperazine maleate
34 4Propranolol Hydrochloride
35 4Sodium Ibandronate Monohydrate
36 4Solriamfetol Hydrochloride
37 2Solriamfetol hydrochloride
38 2Sunny Day
39 2Thiotepa
01 12ATNAHS PHARMA NETHERLANDS BV
02 1ATNAHS PHARMA UK LIMITED
03 1ATNAHS PHARMA UK LTD
04 9ATNAHS PHARMA US
05 25Atnahs Pharma Netherlands BV
06 12Atnahs Pharma Netherlands Bv
07 25Atnahs Pharma Netherlands Bv.
08 37Atnahs Pharma Switzerland Ag
09 3Atnahs Pharma Uk Ltd.
01 5Capsule
02 2Concentrate For Infusion Solution
03 9Concentrate For Solution For Infusion
04 31Film Coated Tablet
05 3Film-Coated Tablets
06 1Granule For Oral Suspension
07 2Granules
08 1Hard Capsules
09 7Injectable Solution
10 1Injection Solution
11 1Ketorolac 30Mg 3 Units' Parenteral Use
12 2Powder For Concentrate For Solution For Infusion
13 1SOLUTION
14 1SUSPENSION;ORAL
15 2Soft Capsule
16 2Soft Capsules
17 7Solution For Injection
18 1Solution For Perfusion
19 2TABLET, DELAYED RELEASE;ORAL
20 6TABLET;ORAL
21 34Tablet
22 4Tablets
01 10.25 mcg
02 10.25MCG
03 30.25mcg
04 10.5 mcg
05 10.5MCG
06 10.5MG
07 10.5mcg
08 11 mg
09 11.0mg/ml
10 1100 mg
11 1100 mg + 25 mg
12 1100MG
13 1100mg
14 1100mg;25mg
15 110MCG
16 510MG
17 110MG/ML
18 910mg
19 110mg/10ml
20 110mg/ml
21 1125mg
22 1150 mg
23 1150MG
24 7150mg
25 115MG
26 31MG
27 11mg
28 11mg/ml
29 12 mg
30 120 mg
31 120 mg+12.5 mg
32 220MG
33 320mg
34 120mg; 12.5mg
35 120mg;12.5mg
36 1250MG
37 3250mg
38 125MG/ML
39 125mg
40 12MG
41 12mg
42 22mg/2ml
43 13 VIALS IM EV 30 mg 1 ml
44 130 mg/ml
45 330mg/ml
46 2375MG
47 13MG
48 13mg
49 23mg/3ml
50 140MG
51 140mg
52 15 mg
53 2500MG
54 3500mg
55 150MCG
56 150MG
57 550mg
58 150mg + 12.5mg
59 150mg;12.5mg
60 1550MG
61 1550mg
62 15MG
63 25mg
64 15mg/ml
65 160MG
66 260mg
67 36mg/6ml
68 175MG
69 375mg
70 1EQ 250MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
71 1EQ 500MG BASE
72 9Blank
01 1Canada
02 12Denmark
03 13Italy
04 3Moldova
05 25Norway
06 25Spain
07 37Switzerland
08 9USA
Regulatory Info :
Registration Country : Italy
Dosage Form : Tablets
Brand Name : TENORMIN
Dosage Strength : 100 mg
Packaging : 42 UNITS 100 MG - ORAL USE
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Italy
Regulatory Info : Allowed
Registration Country : Switzerland
Dosage Form : Tablet
Brand Name : Tenormin mite
Dosage Strength : 50mg
Packaging :
Approval Date : 19/08/1976
Application Number : 39879
Regulatory Info : Allowed
Registration Country : Switzerland
Regulatory Info : Allowed
Registration Country : Switzerland
Dosage Form : Tablet
Brand Name : Tenormin
Dosage Strength : 100mg
Packaging :
Approval Date : 19/08/1976
Application Number : 39879
Regulatory Info : Allowed
Registration Country : Switzerland
Regulatory Info : Allowed
Registration Country : Switzerland
Dosage Form : Tablet
Brand Name : Tenormin submit
Dosage Strength : 25mg
Packaging :
Approval Date : 19/08/1976
Application Number : 39879
Regulatory Info : Allowed
Registration Country : Switzerland
Regulatory Info : Authorized
Registration Country : Spain
Dosage Form : Injectable Solution
Brand Name : Tenormin
Dosage Strength : 0.5MG
Packaging :
Approval Date : 01-05-1987
Application Number : 56777
Regulatory Info : Authorized
Registration Country : Spain
Regulatory Info : Authorized
Registration Country : Spain
Dosage Form : Tablet
Brand Name : Tenormin
Dosage Strength : 50MG
Packaging :
Approval Date : 01-04-1986
Application Number : 56967
Regulatory Info : Authorized
Registration Country : Spain
Regulatory Info :
Registration Country : Italy
Dosage Form : Tablet
Brand Name : TENORTIC
Dosage Strength : 100 mg + 25 mg
Packaging : 28 UNITS (100+25) MG - ORAL USE
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Italy
Regulatory Info :
Registration Country : Italy
Dosage Form : Tablet
Brand Name : TENORTIC
Dosage Strength : 50mg + 12.5mg
Packaging : 28 UNITS (50+12.5) MG - ORAL USE
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Italy
Regulatory Info : Allowed
Registration Country : Switzerland
Dosage Form : Film Coated Tablet
Brand Name : Tenoretic mite
Dosage Strength : 50mg;12.5mg
Packaging :
Approval Date : 10/12/1979
Application Number : 42204
Regulatory Info : Allowed
Registration Country : Switzerland
Regulatory Info : Allowed
Registration Country : Switzerland
Dosage Form : Film Coated Tablet
Brand Name : Tenoretic
Dosage Strength : 100mg;25mg
Packaging :
Approval Date : 10/12/1979
Application Number : 42204
Regulatory Info : Allowed
Registration Country : Switzerland
