Orange Book product · Generic (ANDA)
OCTREOTIDE ACETATE
OCTREOTIDE ACETATE
At a glance
Apr 08, 2005
Approved
Generic (ANDA)
Application
AP
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
Apr 08, 2005
21 yr 6 mo ago
Today
Pharmaceutical detail
Active ingredient
OCTREOTIDE ACETATE
Strength
EQ 0.2MG BASE/ML
Dosage form
INJECTABLE
Route
INJECTION
TE code
AP
Application
ANDA 076330
Product number
001
Marketing status
RX
Reference listed drug (RLD)
No
Reference standard (RS)
Yes
Active-ingredient family
View full familyGeneric (ANDA) of OCTREOTIDE ACETATE
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ANDA 216589 · MYLAN LABS LTD
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ANDA 217860 · SHUANGCHENG
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ANDA 210317 · TEVA PHARMS USA INC
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ANDA 216839 · GLAND
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ANDA 216807 · GLAND
- 2018OCTREOTIDE ACETATEGeneric (ANDA)
ANDA 204669 · HERITAGE
- 2018OCTREOTIDE ACETATEGeneric (ANDA)
ANDA 203765 · HERITAGE
- 2013OCTREOTIDE ACETATEGeneric (ANDA)
ANDA 091041 · SAGENT PHARMS INC
Listed patents
No patents are listed against this product in the Orange Book. Listed patents reflect those the NDA holder submits under 21 U.S.C. 355 and are not exhaustive.

