01 1AZITHROMYCIN
02 1CALCIUM CHLORIDE
03 1CLINDAMYCIN PALMITATE HYDROCHLORIDE
04 1FLUDARABINE PHOSPHATE
05 5FLUOROURACIL
06 2IFOSFAMIDE
07 1LIDOCAINE HYDROCHLORIDE
08 4Lacosamide
09 1METHOTREXATE SODIUM
10 1POLYETHYLENE GLYCOL 3350; POTASSIUM CHLORIDE; SODIUM BICARBONATE; SODIUM CHLORIDE
11 1POLYETHYLENE GLYCOL 3350; POTASSIUM CHLORIDE; SODIUM BICARBONATE; SODIUM CHLORIDE; SODIUM SULFATE ANHYDROUS
12 4PROPRANOLOL HYDROCHLORIDE
13 2SODIUM ACETATE
14 1Sugammadex
15 2Sugammadex Sodium
16 6TEMOZOLOMIDE
17 2TRIAMCINOLONE ACETONIDE
01 29EXTROVIS
02 7Extrovis Eu Kft.
01 4CAPSULE, EXTENDED RELEASE;ORAL
02 6CAPSULE;ORAL
03 3CREAM;TOPICAL
04 3FOR SOLUTION;ORAL
05 6INJECTABLE;INJECTION
06 2Infusion Solution
07 1Injectable Solution
08 1Injection Solution
09 2OINTMENT;TOPICAL
10 2SOLUTION;INTRAVENOUS
11 2SOLUTION;TOPICAL
12 1Solution For Infusion
13 1Solution For Injection
14 1Solution For Perfusion
15 1TABLET;ORAL
01 10.025% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
02 10.1% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
03 20.5%
04 1100MEQ/50ML (2MEQ/ML)
05 1100MG
06 1100MG/ML
07 3100mg/ml
08 110MG
09 310mg/ml
10 1120MG
11 1140MG
12 1160MG
13 1180MG
14 11GM/20ML (50MG/ML)
15 22%
16 1200MEQ/100ML (2MEQ/ML)
17 120MG
18 1236GM/BOT;2.97GM/BOT;6.74GM/BOT;5.86GM/BOT;22.74GM/BOT
19 1250MG
20 13GM/60ML (50MG/ML)
21 1420GM/BOT;1.48GM/BOT;5.72GM/BOT;11.2GM/BOT
22 15%
23 15% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
24 150MG/2ML (25MG/ML)
25 15MG
26 160MG
27 180MG
28 1EQ 1GM BASE/40ML (EQ 25MG BASE/ML)
29 1EQ 500MG BASE
30 1EQ 75MG BASE/5ML
01 2Denmark
02 2Estonia
03 1Spain
04 2Sweden
05 29USA
Regulatory Info : DISCN
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : AZITHROMYCIN
Dosage Strength : EQ 500MG BASE
Packaging :
Approval Date : 2007-05-30
Application Number : 65366
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : INJECTABLE;INJECTION
Brand Name : CALCIUM CHLORIDE 10%
Dosage Strength : 100MG/ML
Packaging :
Approval Date : 2024-11-27
Application Number : 219342
Regulatory Info : RX
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
CLINDAMYCIN PALMITATE HYDROCHLORIDE
Dosage Form : FOR SOLUTION;ORAL
Brand Name : CLINDAMYCIN PALMITATE HYD...
Dosage Strength : EQ 75MG BASE/5ML
Packaging :
Approval Date : 2016-05-25
Application Number : 203063
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Dosage Form : INJECTABLE;INJECTION
Brand Name : FLUDARABINE PHOSPHATE
Dosage Strength : 50MG/2ML (25MG/ML)
Packaging :
Approval Date : 2011-12-21
Application Number : 200647
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : SOLUTION;TOPICAL
Brand Name : EFUDEX
Dosage Strength : 2%
Packaging :
Approval Date : 1982-01-01
Application Number : 16831
Regulatory Info : RX
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Dosage Form : SOLUTION;TOPICAL
Brand Name : EFUDEX
Dosage Strength : 5% **Federal Register ...
Packaging :
Approval Date : 1982-01-01
Application Number : 16831
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : CREAM;TOPICAL
Brand Name : EFUDEX
Dosage Strength : 5%
Packaging :
Approval Date : 1982-01-01
Application Number : 16831
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : CREAM;TOPICAL
Brand Name : CARAC
Dosage Strength : 0.5%
Packaging :
Approval Date : 2000-10-27
Application Number : 20985
Regulatory Info : RX
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Dosage Form : CREAM;TOPICAL
Brand Name : FLUOROURACIL
Dosage Strength : 0.5%
Packaging :
Approval Date : 2015-04-20
Application Number : 203122
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Dosage Form : INJECTABLE;INJECTION
Brand Name : IFOSFAMIDE
Dosage Strength : 1GM/20ML (50MG/ML)
Packaging :
Approval Date : 2012-11-26
Application Number : 201689
Regulatory Info : DISCN
Registration Country : USA
Extrovis Ag is a supplier offers 9 products (APIs, Excipients or Intermediates).
Find Dapsone bulk with DMF, CEP offered by Extrovis Ag
Find Avibactam Sodium bulk with DMF offered by Extrovis Ag
Find Calcium Gluconate bulk with DMF offered by Extrovis Ag
Find Eltrombopag bulk with DMF offered by Extrovis Ag
Find Potassium Dihydrogen Phosphate bulk with DMF offered by Extrovis Ag
Find Potassium Phosphate bulk with DMF offered by Extrovis Ag
Find Tolvaptan bulk with DMF offered by Extrovis Ag
Find Trabectedin bulk with DMF offered by Extrovis Ag
Find Sugammadex Sodium bulk offered by Extrovis Ag
