01 4Aspen Pharmacare Holdings
02 1Dr. Reddy's Laboratories
03 1ABRAXIS PHARM
04 2Abboxia AB
05 4Actavis Inc
06 5Akciju sabiedriba Kalceks
07 2Alcon Inc
08 2Amneal Pharmaceuticals
09 1Amphastar Pharmaceuticals
10 3Aurobindo Pharma Limited
11 6Bausch & Lomb Incorporated
12 1Belmar Pharma Solutions
13 2Bharat Parenterals Limited
14 1CENT PHARMS
15 1Dell Environmental Monitoring Centre
16 2Epic Pharma. LLC.
17 4Farbe Firma
18 1Flagship Biotech International Pvt. Ltd
19 6Fresenius Kabi USA
20 1Fresenius SE & Co. KGaA
21 2GENEYORK PHARMS
22 2GLAND PHARMA LIMITED
23 4Galepharma
24 3Ha Noi CPC1 Pharmaceutical JSC
25 2Hameln Pharma GmbH
26 1Harson Laboratories
27 1Health Biotech
28 3Hikma Pharmaceuticals
29 3IBN Savio
30 1Igenius Life Sciences
31 2Ind Swift Laboratories Limited
32 1Infugen Pharma
33 1Instituto Biologico Contemporaneo
34 1LYPHOMED
35 1Laboratoires Thea
36 1Lifespan Biotech
37 1Luitpold Pharmaceuticals, Inc.
38 8Merck & Co
39 2Mercury Laboratories
40 1Micro Labs Limited
41 1Montage Laboratories
42 3Omega Laboratories Limited
43 1PHARMA STULLN INC.
44 1Pharma Swede
45 3Pharmascience Inc.
46 2Pluviaendo
47 4Quad Pharma
48 2Rosemont
49 2SIFI
50 3SIT LABORATORIO FARMAC. Srl
51 2SOLA BARNES HIND
52 1STERIMAX INC
53 3Sandoz B2B
54 3Somerset Pharmaceuticals Inc
55 2Teva Pharmaceutical Industries
56 1Thea Pharma
57 1Trinity Pharmaceuticals
58 2UCB Pharma S.A
59 1URSAPHARM Arzneimittel GmbH
60 1Umedica Laboratories
61 2VETOQUINOL N A INC
62 2Viatris
63 2Vital Pharma Nordic ApS
64 1Wyeth Pharmaceuticals Inc
65 3Zhejiang Xianju Pharmaceutical Co. Ltd
01 1AEROSOL, METERED;INHALATION
02 1AEROSOL;NASAL
03 1Ampoule
04 1CREAM;TOPICAL
05 1DROPS
06 1EED
07 1EYE DROPS, SOLUTION
08 2Gtt Opht
09 2INJ
10 46INJECTABLE;INJECTION
11 3INJECTION
12 4Inj Sol
13 4Injectable; Injection
14 19Injection
15 2Injection
16 4LIQUID
17 1Liquid Injection
18 4OINTMENT;OPHTHALMIC
19 1OPG
20 2ORAL SOLUTION
21 3Ophthalmic Solution
22 1Parenteral Suspension
23 7SOLUTION
24 7SOLUTION/DROPS;OPHTHALMIC
25 3SOLUTION/DROPS;OPHTHALMIC, OTIC
26 1SOLUTION/DROPS;OTIC
27 2Solution for injection
28 9Solution for injection/infusion
29 1Vial
30 5Blank
01 43DISCN
02 6Generic
03 2OTC
04 2Originator
05 10Prescription
06 21RX
07 56Blank
01 3Cortiarscolloid
02 8DECADRON
03 1DECADRON W/ XYLOCAINE
04 1DEXACEN-4
05 2DEXACORT
06 2DEXAIR
07 3DEXAMETHASONE
08 1DEXAMETHASONE 2 STERILE INJECTABLE SOLUTION
09 1DEXAMETHASONE 5 STERILE INJECTABLE SOLUTION
10 1DEXAMETHASONE OMEGA UNIDOSE
11 1DEXAMETHASONE SOD PHOSPH INJ 10MG/ML USP
12 43DEXAMETHASONE SODIUM PHOSPHATE
13 1DEXAMETHASONE SODIUM PHOSPHATE INJ USP 4MG/ML
14 1DEXAMETHASONE SODIUM PHOSPHATE INJECTION, USP
15 3DEXAMETHASONE SODIUM PHOSPHATE PRESERVATIVE FREE
16 2DEXAMETHASONE-OMEGA
17 2Dexacur
18 1Dexafree
19 1Dexagel
20 1Dexagenta-POS
21 1Dexalevo-drop
22 4Dexamethasone Galepharm Amp
23 1Dexamethasone Sodium Phosphate
24 2Dexamethasone phosphate Hameln
25 5Dexamethasone phosphate Kalceks
26 1Dexamoxi
27 1Dexaphan
28 2Dexavit
29 1EUDEX
30 1Fresenius Dexamethasone 4 mg/1 ml
31 3HEXADROL
32 1MAXIDEX
33 2NEODECADRON
34 1NEOMYCIN SULFATE AND DEXAMETHASONE SODIUM PHOSPHATE
35 2NEOMYCIN SULFATE-DEXAMETHASONE SODIUM PHOSPHATE
36 2Netildex
37 1PMS-DEXAMETHASONE SOD PHOSPHATE DPS 1MG/ML
38 1PMS-DEXAMETHASONE SOD PHOSPHATE INJ 10MG/ML
39 1PMS-DEXAMETHASONE SOD PHOSPHATE INJ 4MG/ML
40 1Spersadex comp.
41 2Stedex
42 1Tagalon 4 mg/ml
43 1Tobrameson
44 1Voxidex
45 2dexamethasone
46 20Blank
01 1Argentina
02 12Canada
03 3China
04 1Egypt
05 18India
06 8Italy
07 11Norway
08 4South Africa
09 3Sweden
10 6Switzerland
11 2Turkey
12 68USA
13 3Vietnam
Regulatory Info : DISCN
Registration Country : USA
DEXAMETHASONE SODIUM PHOSPHATE
Brand Name : HEXADROL
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 4MG PHOSPHATE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1982-01-01
Application Number : 14694
Regulatory Info : DISCN
Registration Country : USA
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
Regulatory Info : DISCN
Registration Country : USA
DEXAMETHASONE SODIUM PHOSPHATE
Brand Name : DEXAMETHASONE SODIUM PHOSPHATE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 4MG PHOSPHATE/ML
Packaging :
Approval Date : 1986-04-09
Application Number : 89169
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
DEXAMETHASONE SODIUM PHOSPHATE
Brand Name : HEXADROL
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 10MG PHOSPHATE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1982-01-01
Application Number : 14694
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
DEXAMETHASONE SODIUM PHOSPHATE
Brand Name : HEXADROL
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 20MG PHOSPHATE/ML
Packaging :
Approval Date : 1982-01-01
Application Number : 14694
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : Originator
Registration Country : South Africa
Dexamethasone sodium phosphate
Brand Name : Voxidex
Dosage Form : EED
Dosage Strength : 1mg/ml
Packaging : 1X1mg/ml
Approval Date :
Application Number :
Regulatory Info : Originator
Registration Country : South Africa
Regulatory Info : RX
Registration Country : USA
DEXAMETHASONE SODIUM PHOSPHATE
Brand Name : DEXAMETHASONE SODIUM PHOSPHATE
Dosage Form : SOLUTION/DROPS;OPHTHALMIC, OTIC
Dosage Strength : EQ 0.1% PHOSPHATE
Packaging :
Approval Date : 1996-07-26
Application Number : 40069
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
DEXAMETHASONE SODIUM PHOSPHATE
Brand Name : DEXAMETHASONE SODIUM PHOSPHATE PRESERVATIVE FREE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 10MG PHOSPHATE/ML
Packaging :
Approval Date : 2003-04-11
Application Number : 40491
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
DEXAMETHASONE SODIUM PHOSPHATE
Brand Name : DEXAMETHASONE SODIUM PHOSPHATE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 10MG PHOSPHATE/ML
Packaging :
Approval Date : 2005-04-22
Application Number : 40572
Regulatory Info : RX
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
DEXAMETHASONE SODIUM PHOSPHATE
Brand Name : DECADRON
Dosage Form : OINTMENT;OPHTHALMIC
Dosage Strength : EQ 0.05% PHOSPHATE
Packaging :
Approval Date : 1982-01-01
Application Number : 11977
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
DEXAMETHASONE SODIUM PHOSPHATE
Brand Name : DECADRON
Dosage Form : CREAM;TOPICAL
Dosage Strength : EQ 0.1% PHOSPHATE
Packaging :
Approval Date : 1982-01-01
Application Number : 11983
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
DEXAMETHASONE SODIUM PHOSPHATE
Brand Name : DECADRON
Dosage Form : SOLUTION/DROPS;OPHTHALMIC, OTIC
Dosage Strength : EQ 0.1% PHOSPHATE
Packaging :
Approval Date : 1982-01-01
Application Number : 11984
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
DEXAMETHASONE SODIUM PHOSPHATE
Brand Name : DECADRON
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 4MG PHOSPHATE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1982-01-01
Application Number : 12071
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
DEXAMETHASONE SODIUM PHOSPHATE
Brand Name : DECADRON
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 24MG PHOSPHATE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1982-01-01
Application Number : 12071
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
DEXAMETHASONE SODIUM PHOSPHATE; LIDOCAINE HYDROCHLORIDE
Brand Name : DECADRON W/ XYLOCAINE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 4MG PHOSPHATE/ML;10MG/ML
Packaging :
Approval Date : 1982-01-01
Application Number : 13334
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
DEXAMETHASONE SODIUM PHOSPHATE; NEOMYCIN SULFATE
Brand Name : NEODECADRON
Dosage Form : SOLUTION/DROPS;OPHTHALMIC
Dosage Strength : EQ 0.1% PHOSPHATE;EQ 3.5MG BASE/ML
Packaging :
Approval Date : 1982-01-01
Application Number : 50322
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
DEXAMETHASONE SODIUM PHOSPHATE; NEOMYCIN SULFATE
Brand Name : NEODECADRON
Dosage Form : OINTMENT;OPHTHALMIC
Dosage Strength : EQ 0.05% PHOSPHATE;EQ 3.5MG BASE/GM
Packaging :
Approval Date : 1982-01-01
Application Number : 50324
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
DEXAMETHASONE SODIUM PHOSPHATE
Brand Name : DEXACORT
Dosage Form : AEROSOL, METERED;INHALATION
Dosage Strength : EQ 0.1MG PHOSPHATE/INH
Packaging :
Approval Date : 1982-01-01
Application Number : 13413
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
DEXAMETHASONE SODIUM PHOSPHATE
Brand Name : DEXACORT
Dosage Form : AEROSOL;NASAL
Dosage Strength : EQ 0.1MG PHOSPHATE/INH
Packaging :
Approval Date : 1982-01-01
Application Number : 14242
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
DEXAMETHASONE SODIUM PHOSPHATE
Brand Name : DEXAMETHASONE SODIUM PHOSPHATE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 10MG PHOSPHATE/ML
Packaging :
Approval Date : 2008-08-29
Application Number : 40802
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
DEXAMETHASONE SODIUM PHOSPHATE
Brand Name : DEXAMETHASONE SODIUM PHOSPHATE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 4MG PHOSPHATE/ML
Packaging :
Approval Date : 2008-08-29
Application Number : 40803
Regulatory Info : RX
Registration Country : USA
