01 6Atenolol
02 4Atenolol; Chlorthalidone
03 6Calcitriol
04 2Cladribine
05 3Clobazam
06 8Diazepam
07 3Famciclovir
08 4Granisetron
09 3Granisetron Hydrochloride
10 2Granisetrone
11 1Ibandronate sodium
12 5Ibandronic Acid
13 2KETOROLAC TROMETHAMINE
14 3Ketorolac
15 3Ketorolac Trometamol
16 6Lisinopril
17 3Lisinopril; Hydrochlorothiazide
18 8Lisinoprildihydrat
19 1Macimorelin Acetate
20 1Macimorelinacetat
21 6NAPROXEN
22 2NAPROXEN SODIUM
23 1Naproxen
24 1Naproxen Sodium
25 3Olsalazine
26 4Propranolol Hydrochloride
27 2Solriamfetol Hydrochloride
28 2Solriamfetol hydrochloride
29 2Sunny Day
30 2Thiotepa
01 12ATNAHS PHARMA NETHERLANDS BV
02 1ATNAHS PHARMA UK LIMITED
03 1ATNAHS PHARMA UK LTD
04 9ATNAHS PHARMA US
05 13Atnahs Pharma Netherlands BV
06 22Atnahs Pharma Netherlands Bv.
07 37Atnahs Pharma Switzerland Ag
08 4Atnahs Pharma UK Limited
01 2Antic-calc Tablet
02 2Capsule
03 1Capsule, hard
04 5Concentrate For Solution For Infusion
05 21Film Coated Tablet
06 3Film-Coated Tablets
07 1Granule For Oral Suspension
08 1Granules for oral solution, suspension in sachet
09 5Injectable Solution
10 1Injection fluid, resolution
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 4Solution For Injection
18 1Solution For Perfusion
19 2TABLET, DELAYED RELEASE;ORAL
20 6TABLET;ORAL
21 29Tablet
22 2Tablet, film-coated
23 4Tablets
01 10.25 mcg
02 10.25MCG
03 10.25mcg
04 10.5 mcg
05 10.5MCG
06 10.5MG
07 10.5mcg
08 11 mg
09 11.0mg/ml
10 310 mg
11 1100 mg
12 1100 mg + 25 mg
13 1100MG
14 1100mg
15 1100mg;25mg
16 510MG
17 110MG/ML
18 510mg
19 110mg/10ml
20 110mg/ml
21 1125mg
22 2150 mg
23 1150MG
24 2150mg
25 115MG
26 31MG
27 11mg
28 12 mg
29 320 mg
30 120 mg+12.5 mg
31 220MG
32 120mg
33 120mg;12.5mg
34 1250 mg
35 1250MG
36 1250mg
37 125MG/ML
38 125mg
39 12mg
40 12mg/2ml
41 13 VIALS IM EV 30 mg 1 ml
42 230 mg/ml
43 130mg/ml
44 2375MG
45 13MG
46 23mg/3ml
47 140MG
48 140mg
49 65 mg
50 2500 mg
51 2500MG
52 1500mg
53 150MG
54 250mg
55 150mg + 12.5mg
56 150mg;12.5mg
57 1550MG
58 1550mg
59 15MG
60 25mg
61 15mg/ml
62 160 mg
63 160MG
64 16mg/6ml
65 175 mg
66 175MG
67 175mg
68 1EQ 250MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
69 1EQ 500MG BASE
70 1Blank
01 1Canada
02 13Italy
03 17Norway
04 22Spain
05 37Switzerland
06 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
