01 6Atenolol
02 4Atenolol; Chlorthalidone
03 8Calcitriol
04 2Cladribine
05 3Clobazam
06 8Diazepam
07 3Famciclovir
08 4Granisetron
09 3Granisetron Hydrochloride
10 2Granisetrone
11 1Ibandronate sodium
12 5Ibandronate sodium monohydrate
13 5Ibandronic Acid
14 3Ibandronic acid
15 2KETOROLAC TROMETHAMINE
16 2Ketorolac
17 3Ketorolac Trometamol
18 1Ketorolaktrometamol
19 6Lisinopril
20 8Lisinopril dihydrate
21 1Lisinopril dihydrate; Hydrochlorothiazide
22 3Lisinopril; Hydrochlorothiazide
23 1Macimorelin Acetate
24 1Macimorelin acetate
25 6NAPROXEN
26 2NAPROXEN SODIUM
27 1Naproxen
28 1Naproxen Sodium
29 2Olsalazine sodium
30 1Prochlorperazine maleate
31 4Propranolol Hydrochloride
32 2Solriamfetol Hydrochloride
33 2Solriamfetol hydrochloride
34 2Sunny Day
35 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 22Atnahs Pharma Netherlands Bv.
07 37Atnahs Pharma Switzerland Ag
08 3Atnahs Pharma Uk Ltd.
01 5Capsule
02 7Concentrate For Solution For Infusion
03 27Film Coated Tablet
04 3Film-Coated Tablets
05 1Granule For Oral Suspension
06 1Granules
07 6Injectable Solution
08 1Ketorolac 30Mg 3 Units' Parenteral Use
09 2Powder For Concentrate For Solution For Infusion
10 1SOLUTION
11 1SUSPENSION;ORAL
12 2Soft Capsule
13 2Soft Capsules
14 6Solution For Injection
15 1Solution For Perfusion
16 2TABLET, DELAYED RELEASE;ORAL
17 6TABLET;ORAL
18 32Tablet
19 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 510MG
16 110MG/ML
17 810mg
18 110mg/10ml
19 110mg/ml
20 1125mg
21 1150 mg
22 1150MG
23 5150mg
24 115MG
25 31MG
26 11mg
27 12 mg
28 120 mg
29 120 mg+12.5 mg
30 220MG
31 320mg
32 120mg; 12.5mg
33 120mg;12.5mg
34 1250MG
35 2250mg
36 125MG/ML
37 125mg
38 12mg
39 12mg/2ml
40 13 VIALS IM EV 30 mg 1 ml
41 130 mg/ml
42 230mg/ml
43 2375MG
44 13MG
45 13mg
46 23mg/3ml
47 140MG
48 140mg
49 15 mg
50 2500MG
51 2500mg
52 150MG
53 450mg
54 150mg + 12.5mg
55 150mg;12.5mg
56 1550MG
57 1550mg
58 15MG
59 25mg
60 15mg/ml
61 160MG
62 160mg
63 26mg/6ml
64 175MG
65 275mg
66 1EQ 250MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
67 1EQ 500MG BASE
68 9Blank
01 1Canada
02 13Italy
03 3Moldova
04 25Norway
05 22Spain
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 : 1987-05-01
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 : 1986-04-01
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
