01 1CHIESI
02 5FRESENIUS KABI USA
03 4GLAND PHARMA LTD
04 5HERITAGE
05 5MEITHEAL
06 3MYLAN INSTITUTIONAL
07 8NOVARTIS
08 5SAGENT PHARMS INC
09 1SHUANGCHENG
10 1SUN PHARM
11 10SUN PHARM INDS
12 3TEVA PHARMS USA INC
13 5WEST-WARD PHARMS INT
14 5WOCKHARDT USA
01 1CAPSULE, DELAYED RELEASE;ORAL
02 59INJECTABLE;INJECTION
03 1SOLUTION;SUBCUTANEOUS
01 18DISCN
02 43RX
01 1BYNFEZIA PEN
02 1MYCAPSSA
03 36OCTREOTIDE ACETATE
04 12OCTREOTIDE ACETATE (PRESERVATIVE FREE)
05 3OCTREOTIDE ACETATE PRESERVATIVE FREE
06 5SANDOSTATIN
07 3SANDOSTATIN LAR
01 51No
02 10Yes
RLD : No
TE Code : AP
Brand Name : OCTREOTIDE ACETATE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 0.05MG BASE/ML
Approval Date : 2005-10-03
Application Number : 75957
RX/OTC/DISCN : RX
RLD : No
TE Code : AP
RLD : No
TE Code : AP
Brand Name : OCTREOTIDE ACETATE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 0.1MG BASE/ML
Approval Date : 2005-10-03
Application Number : 75957
RX/OTC/DISCN : RX
RLD : No
TE Code : AP
RLD : Yes
TE Code : AP
Brand Name : SANDOSTATIN
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 0.05MG BASE/ML
Approval Date : 1988-10-21
Application Number : 19667
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AP
RLD : Yes
TE Code : AP
Brand Name : SANDOSTATIN
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 0.1MG BASE/ML
Approval Date : 1988-10-21
Application Number : 19667
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AP
RLD : Yes
TE Code : AP
Brand Name : SANDOSTATIN
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 0.5MG BASE/ML
Approval Date : 1988-10-21
Application Number : 19667
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AP
RLD : Yes
TE Code :
Brand Name : SANDOSTATIN
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 0.2MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1991-06-12
Application Number : 19667
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Brand Name : SANDOSTATIN
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 1MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1991-06-12
Application Number : 19667
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code : AB
Brand Name : SANDOSTATIN LAR
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 10MG BASE/VIAL
Approval Date : 1998-11-25
Application Number : 21008
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AB
RLD : Yes
TE Code : AB
Brand Name : SANDOSTATIN LAR
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 20MG BASE/VIAL
Approval Date : 1998-11-25
Application Number : 21008
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AB
RLD : Yes
TE Code : AB
Brand Name : SANDOSTATIN LAR
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 30MG BASE/VIAL
Approval Date : 1998-11-25
Application Number : 21008
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AB
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