01 2CITRIC ACID; MAGNESIUM OXIDE; SODIUM PICOSULFATE
02 1CORTICORELIN OVINE TRIFLUTATE
03 2DEGARELIX ACETATE
04 15DESMOPRESSIN ACETATE
05 1DINOPROSTONE
06 2GONADORELIN ACETATE
07 9GONADOTROPIN, CHORIONIC
08 3MENOTROPINS (FSH;LH)
09 2PROGESTERONE
10 1PROTIRELIN
11 1SECRETIN
12 3SOMATROPIN
13 2UROFOLLITROPIN
01 1FOR SOLUTION;ORAL
02 20INJECTABLE;INJECTION
03 2INJECTABLE;INTRAMUSCULAR, SUBCUTANEOUS
04 1INJECTABLE;SUBCUTANEOUS
05 1INSERT, EXTENDED RELEASE;VAGINAL
06 1INSERT;VAGINAL
07 1Injectable; Subcutaneous
08 2POWDER;SUBCUTANEOUS
09 2SOLUTION;NASAL
10 1SOLUTION;ORAL
11 5SPRAY, METERED;NASAL
12 1SYSTEM;VAGINAL
13 4TABLET;ORAL
14 2TABLET;SUBLINGUAL
01 10.004MG/ML
02 20.01%
03 10.015MG/ML
04 20.01MG/SPRAY
05 10.01MG/SPRAY **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
06 10.0277MG
07 10.0553MG
08 20.15MG/SPRAY
09 20.1MG
10 20.2MG
11 10.5MG/ML
12 10.8MG/VIAL
13 10.9%
14 11.78GM
15 210,000 UNITS/VIAL
16 1100MG
17 110MG
18 110MG/VIAL
19 112GM/BOT;3.5GM/BOT;10MG/BOT
20 112GM/PACKET;3.5GM/PACKET;10MG/PACKET **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
21 115,000 UNITS/VIAL
22 1150 IU/VIAL;150 IU/VIAL
23 22,000 UNITS/VIAL
24 220,000 UNITS/VIAL
25 13.2MG/VIAL
26 14.8MG/VIAL
27 25,000 UNITS/VIAL
28 15MG/VIAL
29 175 IU/VIAL
30 275 IU/VIAL;75 IU/VIAL
31 175CU/VIAL
32 1EQ 0.1MG BASE/VIAL
33 1EQ 120MG BASE/VIAL
34 1EQ 80MG BASE/VIAL
01 18DISCN
02 8RX
03 18Blank
RLD : Yes
TE Code :
CITRIC ACID; MAGNESIUM OXIDE; SODIUM PICOSULFATE
Dosage Form : FOR SOLUTION; ORAL
Proprietary Name : PREPOPIK
Dosage Strength : 12GM/PACKET;3.5GM/PACKET...
Approval Date : 2012-07-16
Application Number : 202535
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
CITRIC ACID; MAGNESIUM OXIDE; SODIUM PICOSULFATE
Dosage Form : SOLUTION; ORAL
Proprietary Name : CLENPIQ
Dosage Strength : 12GM/BOT;3.5GM/BOT;10MG/...
Approval Date : 2017-11-28
Application Number : 209589
RX/OTC/DISCN : RX
RLD : Yes
TE Code :
RLD :
TE Code :
Dosage Form : INJECTABLE; INJECTION
Proprietary Name : ACTHREL
Dosage Strength : EQ 0.1MG BASE/VIAL
Approval Date :
Application Number : 20162
RX/OTC/DISCN :
RLD :
TE Code :
RLD : Yes
TE Code :
Dosage Form : POWDER; SUBCUTANEOUS
Proprietary Name : FIRMAGON
Dosage Strength : EQ 80MG BASE/VIAL
Approval Date : 2008-12-24
Application Number : 22201
RX/OTC/DISCN : RX
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Dosage Form : POWDER; SUBCUTANEOUS
Proprietary Name : FIRMAGON
Dosage Strength : EQ 120MG BASE/VIAL
Approval Date : 2008-12-24
Application Number : 22201
RX/OTC/DISCN : RX
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Dosage Form : SOLUTION; NASAL
Proprietary Name : DDAVP
Dosage Strength : 0.01%
Approval Date : 1982-01-01
Application Number : 17922
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Dosage Form : SPRAY, METERED; NASAL
Proprietary Name : DDAVP
Dosage Strength : 0.01MG/SPRAY **Federal R...
Approval Date : 1989-02-06
Application Number : 17922
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Dosage Form : SPRAY, METERED; NASAL
Proprietary Name : DDAVP (NEEDS NO REFRIGER...
Dosage Strength : 0.01MG/SPRAY
Approval Date : 1996-08-07
Application Number : 17922
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : No
TE Code :
Dosage Form : TABLET; ORAL
Proprietary Name : DESMOPRESSIN ACETATE
Dosage Strength : 0.1MG
Approval Date : 2008-05-08
Application Number : 21795
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Dosage Form : TABLET; ORAL
Proprietary Name : DESMOPRESSIN ACETATE
Dosage Strength : 0.2MG
Approval Date : 2008-05-08
Application Number : 21795
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
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