01 1AZITHROMYCIN
02 1CALCIUM CHLORIDE
03 1CLINDAMYCIN PALMITATE HYDROCHLORIDE
04 1FLUDARABINE PHOSPHATE
05 5FLUOROURACIL
06 2IFOSFAMIDE
07 1LIDOCAINE HYDROCHLORIDE
08 1METHOTREXATE SODIUM
09 1POLYETHYLENE GLYCOL 3350; POTASSIUM CHLORIDE; SODIUM BICARBONATE; SODIUM CHLORIDE
10 1POLYETHYLENE GLYCOL 3350; POTASSIUM CHLORIDE; SODIUM BICARBONATE; SODIUM CHLORIDE; SODIUM SULFATE ANHYDROUS
11 4PROPRANOLOL HYDROCHLORIDE
12 2SODIUM ACETATE
13 6TEMOZOLOMIDE
14 2TRIAMCINOLONE ACETONIDE
01 4CAPSULE, EXTENDED RELEASE;ORAL
02 6CAPSULE;ORAL
03 3CREAM;TOPICAL
04 3FOR SOLUTION;ORAL
05 6INJECTABLE;INJECTION
06 2OINTMENT;TOPICAL
07 2SOLUTION;INTRAVENOUS
08 2SOLUTION;TOPICAL
09 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01 10.025% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
02 10.1% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 1120MG
08 1140MG
09 1160MG
10 1180MG
11 11GM/20ML (50MG/ML)
12 22%
13 1200MEQ/100ML (2MEQ/ML)
14 120MG
15 1236GM/BOT;2.97GM/BOT;6.74GM/BOT;5.86GM/BOT;22.74GM/BOT
16 1250MG
17 13GM/60ML (50MG/ML)
18 1420GM/BOT;1.48GM/BOT;5.72GM/BOT;11.2GM/BOT
19 15%
20 15% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
21 150MG/2ML (25MG/ML)
22 15MG
23 160MG
24 180MG
25 1EQ 1GM BASE/40ML (EQ 25MG BASE/ML)
26 1EQ 500MG BASE
27 1EQ 75MG BASE/5ML
01 23DISCN
02 4RX
03 2Blank
RLD : No
TE Code :
Dosage Form : TABLET; ORAL
Proprietary Name : AZITHROMYCIN
Dosage Strength : EQ 500MG BASE
Approval Date : 2007-05-30
Application Number : 65366
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code : AP
Dosage Form : INJECTABLE; INJECTION
Proprietary Name : CALCIUM CHLORIDE 10%
Dosage Strength : 100MG/ML
Approval Date : 2024-11-27
Application Number : 219342
RX/OTC/DISCN : RX
RLD : No
TE Code : AP
RLD : No
TE Code :
CLINDAMYCIN PALMITATE HYDROCHLORIDE
Dosage Form : FOR SOLUTION; ORAL
Proprietary Name : CLINDAMYCIN PALMITATE HY...
Dosage Strength : EQ 75MG BASE/5ML
Approval Date : 2016-05-25
Application Number : 203063
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Dosage Form : INJECTABLE; INJECTION
Proprietary Name : FLUDARABINE PHOSPHATE
Dosage Strength : 50MG/2ML (25MG/ML)
Approval Date : 2011-12-21
Application Number : 200647
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : Yes
TE Code : AT
Dosage Form : SOLUTION; TOPICAL
Proprietary Name : EFUDEX
Dosage Strength : 2%
Approval Date : 1982-01-01
Application Number : 16831
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AT
RLD : Yes
TE Code :
Dosage Form : SOLUTION; TOPICAL
Proprietary Name : EFUDEX
Dosage Strength : 5% **Federal Register de...
Approval Date : 1982-01-01
Application Number : 16831
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code : AB
Dosage Form : CREAM; TOPICAL
Proprietary Name : EFUDEX
Dosage Strength : 5%
Approval Date : 1982-01-01
Application Number : 16831
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AB
RLD : Yes
TE Code :
Dosage Form : CREAM; TOPICAL
Proprietary Name : CARAC
Dosage Strength : 0.5%
Approval Date : 2000-10-27
Application Number : 20985
RX/OTC/DISCN : RX
RLD : Yes
TE Code :
RLD : No
TE Code :
Dosage Form : CREAM; TOPICAL
Proprietary Name : FLUOROURACIL
Dosage Strength : 0.5%
Approval Date : 2015-04-20
Application Number : 203122
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Dosage Form : INJECTABLE; INJECTION
Proprietary Name : IFOSFAMIDE
Dosage Strength : 1GM/20ML (50MG/ML)
Approval Date : 2012-11-26
Application Number : 201689
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
Extrovis Ag is a supplier offers 9 products (APIs, Excipients or Intermediates).
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