DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
01 1Dr. Reddy's Laboratories
02 3Strides Pharma Science
03 3AAIPharma Services Corp.
04 4AHN Pharma
05 2ALTANA
06 1APOZEAL PHARMS
07 2Acme Lifetech
08 16Actavis Inc
09 2Alternova A/S
10 2American Regent
11 3Amneal Pharmaceuticals
12 1Anima Medical Centre
13 3Aurobindo Pharma Limited
14 3Avet Pharmaceuticals
15 4Bausch & Lomb Incorporated
16 2Baxter Healthcare Corporation
17 2Bluefish Pharmaceuticals AB
18 4Chartwell Pharmaceuticals llc
19 2EQL Pharma AB,
20 3Epic Pharma. LLC.
21 1Evertogen
22 4Fresenius Kabi USA
23 3Graviti Pharmaceuticals
24 1Grupo Chemo
25 3HALSEY
26 2Hasco-Lek
27 3Hetero Drugs
28 1Hikma Pharmaceuticals
29 3Hospira, Inc.
30 3IVAX Pharmaceuticals Inc
31 3InvaGen Pharmaceuticals Inc
32 1JSC Pharmproject
33 5KV Pharmaceutical
34 3KVK.Tech
35 1Kolmar Korea Co., Ltd.
36 1Lannett Company, Inc.
37 2Medreich
38 2Merck & Co
39 3Mutual Pharmaceutical Company, Inc.
40 2Neogen N.V.
41 5NorthStar Medical Radioisotopes
42 3Nuvo Pharmaceuticals
43 13ORIFARM GROUP AS
44 1PAI Pharmaceutical Associates
45 3PUREPAC PHARM
46 2Paranova Group AS
47 7Pfizer Inc
48 1Pharma-Q Holdings (Pty) Ltd
49 1Pharmachim AB
50 4Pharmascience Inc.
51 4Pliva Hrvatska
52 3Prinston
53 3QUANTUM PHARMICS
54 3Rising Pharmaceuticals Inc
55 1SEARCHLIGHT PHARMA
56 1SMITH & NEPHEW INC
57 3SUPERPHARM
58 4Sandoz B2B
59 6Solo Pak
60 1Substipharm
61 10Sun Pharmaceutical Industries Limited
62 1Towa Pharma
63 3UCB Nordic A / S
64 2UCB Nordic AS
65 6UCB Pharma S.A
66 3USL PHARMA
67 1UpChen Therapeutics Limited
68 1Viatris
69 2Wellcopharma
70 2Wyeth Pharmaceuticals Inc
71 4Yash Pharma Laboratories
72 4Blank
01 5Antic-calc Tablet, Film Coated
02 6CAPSULE
03 2Coated Tablet
04 2Coated Tablets
05 9FILM COATED PILL
06 2FILM COATED TABLET
07 5FILMDRAGERAD TABLETT
08 3Film Coated Tablet
09 1Film-Coated Tablet
10 1Filmtabl
11 3INJ
12 34INJECTABLE;INJECTION
13 1LIQUID
14 2ORAL SOLUTION
15 2Oral Solution
16 1SYR
17 2SYRUP
18 9SYRUP;ORAL
19 2Syrup
20 2TAB
21 1TABLET
22 102TABLET;ORAL
23 10Tablet
24 8Tablet, film-coated
25 3Blank
01 101DISCN
02 2Generic
03 2Generic DCP Ongoing
04 4Originator
05 4Prescription
06 42RX
07 63Blank
01 6ATARAX
02 2Allderm
03 21Atarax
04 1Atarax 25Mg 25 Film-Coated Tablets
05 1Atarax 25Mg 50 Film-Coated Tablets
06 3Aterax
07 1Aterax 2ml
08 1Atyxine
09 4HYDROXYZINE
10 135HYDROXYZINE HYDROCHLORIDE
11 1HYDROXYZINE HYDROCHLORIDE INJECTION USP
12 2Hydroxizin Alternova
13 2Hydroxyzine Bluefish
14 1Hydroxyzine Bluefish 25Mg 25 Coated Tablets Efg
15 1Hydroxyzine Bluefish 25Mg 50 Coated Tablets Efg
16 1Hydroxyzine EQL Pharma
17 6Hydroxyzine Orifarm
18 2Hydroxyzinum Hasco
19 1Neurax
20 2ORGATRAX
21 1PMS HYDROXYZINE CAP 10MG
22 1PMS HYDROXYZINE CAP 25MG
23 1PMS HYDROXYZINE CAP 50MG
24 1PMS HYDROXYZINE SYR 10MG/5ML
25 1Pharma-Q Hydroxyzine Injection 100,0Mg/2Ml
26 2Pru
27 1Pru 10
28 1Pru 25
29 1Urox Syrup
30 2VISTARIL
31 1hydroxyzine CHEMO®
32 11Blank
01 11Canada
02 1Costa Rica
03 1France
04 2Guatemala
05 10India
06 3Italy
07 13Norway
08 2Poland
09 1Russia
10 6South Africa
11 1South Korea
12 4Spain
13 16Sweden
14 1Switzerland
15 1Taiwan
16 145USA
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
Regulatory Info : DISCN
Registration Country : USA
Brand Name : HYDROXYZINE HYDROCHLORIDE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 50MG/ML
Packaging :
Approval Date : 1982-01-01
Application Number : 85779
Regulatory Info : DISCN
Registration Country : USA
Strides Pharma Science: Pioneering IP-driven formulations for niche finished dosage forms.
Regulatory Info : DISCN
Registration Country : USA
Brand Name : HYDROXYZINE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 10MG
Packaging :
Approval Date : 1982-01-22
Application Number : 87602
Regulatory Info : DISCN
Registration Country : USA
Strides Pharma Science: Pioneering IP-driven formulations for niche finished dosage forms.
Regulatory Info : DISCN
Registration Country : USA
Brand Name : HYDROXYZINE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 25MG
Packaging :
Approval Date : 1982-01-22
Application Number : 87603
Regulatory Info : DISCN
Registration Country : USA
Strides Pharma Science: Pioneering IP-driven formulations for niche finished dosage forms.
Regulatory Info : DISCN
Registration Country : USA
Brand Name : HYDROXYZINE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 50MG
Packaging :
Approval Date : 1982-01-22
Application Number : 87604
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : HYDROXYZINE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 10MG
Packaging :
Approval Date : 2008-06-30
Application Number : 40804
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : HYDROXYZINE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 25MG
Packaging :
Approval Date : 2008-06-30
Application Number : 40804
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : HYDROXYZINE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 50MG
Packaging :
Approval Date : 2008-06-30
Application Number : 40804
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : HYDROXYZINE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 50MG
Packaging :
Approval Date : 2004-12-28
Application Number : 40604
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : HYDROXYZINE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 10MG
Packaging :
Approval Date : 2004-12-28
Application Number : 40604
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : HYDROXYZINE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 25MG
Packaging :
Approval Date : 2004-12-28
Application Number : 40604
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : HYDROXYZINE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 10MG
Packaging :
Approval Date : 2008-05-29
Application Number : 40805
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : HYDROXYZINE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 25MG
Packaging :
Approval Date : 2008-05-29
Application Number : 40805
Regulatory Info : RX
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : HYDROXYZINE HYDROCHLORIDE
Dosage Form : SYRUP;ORAL
Dosage Strength : 10MG/5ML
Packaging :
Approval Date : 1994-10-28
Application Number : 40010
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : HYDROXYZINE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 10MG
Packaging :
Approval Date : 2007-03-20
Application Number : 40786
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : HYDROXYZINE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 25MG
Packaging :
Approval Date : 2007-03-20
Application Number : 40786
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : HYDROXYZINE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 50MG
Packaging :
Approval Date : 2007-03-20
Application Number : 40786
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : HYDROXYZINE HYDROCHLORIDE
Dosage Form : SYRUP;ORAL
Dosage Strength : 10MG/5ML
Packaging :
Approval Date : 2002-04-10
Application Number : 40391
Regulatory Info : RX
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : ATARAX
Dosage Form : TABLET;ORAL
Dosage Strength : 10MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1982-01-01
Application Number : 10392
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : ATARAX
Dosage Form : TABLET;ORAL
Dosage Strength : 25MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1982-01-01
Application Number : 10392
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : ATARAX
Dosage Form : TABLET;ORAL
Dosage Strength : 100MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1982-01-01
Application Number : 10392
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : ATARAX
Dosage Form : TABLET;ORAL
Dosage Strength : 50MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1982-01-01
Application Number : 10392
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : ATARAX
Dosage Form : SYRUP;ORAL
Dosage Strength : 10MG/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1982-01-01
Application Number : 10485
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : VISTARIL
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 25MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1982-01-01
Application Number : 11111
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : VISTARIL
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 50MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1982-01-01
Application Number : 11111
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : HYDROXYZINE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 50MG
Packaging :
Approval Date : 2005-05-27
Application Number : 40580
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : HYDROXYZINE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 25MG
Packaging :
Approval Date : 2005-05-27
Application Number : 40580
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : HYDROXYZINE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 10MG
Packaging :
Approval Date : 2005-05-27
Application Number : 40580
Regulatory Info : RX
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : HYDROXYZINE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 10MG
Packaging :
Approval Date : 2004-07-22
Application Number : 40559
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : HYDROXYZINE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 25MG
Packaging :
Approval Date : 2004-07-22
Application Number : 40562
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : HYDROXYZINE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 50MG
Packaging :
Approval Date : 2004-07-22
Application Number : 40563
Regulatory Info : DISCN
Registration Country : USA
