01 6Atenolol
02 4Atenolol; Chlorthalidone
03 8Calcitriol
04 2Catumaxomab
05 3Cladribine
06 3Clobazam
07 8Diazepam
08 3Famciclovir
09 4Granisetron
10 3Granisetron Hydrochloride
11 2Granisetrone
12 1Ibandronate sodium
13 5Ibandronate sodium monohydrate
14 5Ibandronic Acid
15 3Ibandronic acid
16 2KETOROLAC TROMETHAMINE
17 2Ketorolac
18 3Ketorolac Trometamol
19 1Ketorolaktrometamol
20 6Lisinopril
21 8Lisinopril dihydrate
22 1Lisinopril dihydrate; Hydrochlorothiazide
23 3Lisinopril; Hydrochlorothiazide
24 1Macimorelin Acetate
25 1Macimorelin acetate
26 6NAPROXEN
27 2NAPROXEN SODIUM
28 1Naproxen
29 1Naproxen Sodium
30 2Olsalazine sodium
31 1Prochlorperazine maleate
32 4Propranolol Hydrochloride
33 2Solriamfetol Hydrochloride
34 2Solriamfetol hydrochloride
35 2Sunny Day
36 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 25Atnahs Pharma Netherlands Bv.
07 37Atnahs Pharma Switzerland Ag
08 3Atnahs Pharma Uk Ltd.
01 5Capsule
02 2Concentrate For Infusion Solution
03 7Concentrate For Solution For Infusion
04 27Film Coated Tablet
05 3Film-Coated Tablets
06 1Granule For Oral Suspension
07 1Granules
08 7Injectable Solution
09 1Ketorolac 30Mg 3 Units' Parenteral Use
10 2Powder For Concentrate For Solution For Infusion
11 1SOLUTION
12 1SUSPENSION;ORAL
13 2Soft Capsule
14 2Soft Capsules
15 6Solution For Injection
16 1Solution For Perfusion
17 2TABLET, DELAYED RELEASE;ORAL
18 6TABLET;ORAL
19 32Tablet
20 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 810mg
19 110mg/10ml
20 110mg/ml
21 1125mg
22 1150 mg
23 1150MG
24 5150mg
25 115MG
26 31MG
27 11mg
28 12 mg
29 120 mg
30 120 mg+12.5 mg
31 220MG
32 320mg
33 120mg; 12.5mg
34 120mg;12.5mg
35 1250MG
36 2250mg
37 125MG/ML
38 125mg
39 12MG
40 12mg
41 12mg/2ml
42 13 VIALS IM EV 30 mg 1 ml
43 130 mg/ml
44 230mg/ml
45 2375MG
46 13MG
47 13mg
48 23mg/3ml
49 140MG
50 140mg
51 15 mg
52 2500MG
53 2500mg
54 150MCG
55 150MG
56 450mg
57 150mg + 12.5mg
58 150mg;12.5mg
59 1550MG
60 1550mg
61 15MG
62 25mg
63 15mg/ml
64 160MG
65 160mg
66 26mg/6ml
67 175MG
68 275mg
69 1EQ 250MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
70 1EQ 500MG BASE
71 9Blank
01 1Canada
02 13Italy
03 3Moldova
04 25Norway
05 25Spain
06 37Switzerland
07 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
