01 1ABC HOLDING
02 4ABLE
03 1ACTAVIS ELIZABETH
04 4ACTAVIS LABS FL INC
05 1AUROBINDO PHARMA LTD
06 2AUROLIFE PHARMA LLC
07 1AVANTHI INC
08 3BARR
09 2CAMALL
10 14CHARTWELL RX
11 3CITIUS PHARMS
12 4DR REDDYS LABS SA
13 1DURAMED PHARMS BARR
14 3ELITE LABS
15 5ELITE LABS INC
16 1FERNDALE LABS
17 1GLAXOSMITHKLINE
18 1INGENUS PHARMS LLC
19 5INVAGEN PHARMS
20 2IVAX PHARMS
21 5KVK TECH
22 1KVK TECH INC
23 3LANNETT
24 2LANNETT CO INC
25 3MAST MM
26 4NUVO PHARM
27 1PRINSTON INC
28 1PURACAP LABS BLU
29 10SANDOZ
30 1SANDOZ INC
31 1SHIRE RICHWOOD
32 1SOLVAY
33 1SUN PHARM INDS INC
34 3SUN PHARM INDUSTRIES
35 8TEVA
36 1TG UNITED INC
37 2UPSHER SMITH LABS
38 4USL PHARMA
39 4VITARINE
40 4VIVUS LLC
41 2WATSON LABS
42 3ZYDUS PHARMS
01 12CAPSULE, EXTENDED RELEASE;ORAL
02 1CAPSULE; ORAL
03 70CAPSULE;ORAL
04 6TABLET, ORALLY DISINTEGRATING;ORAL
05 35TABLET;ORAL
01 83DISCN
02 40RX
03 1Blank
01 2ADIPEX-P
02 1FASTIN
03 1LOMAIRA
04 1OBESTIN-30
05 1OBY-TRIM
06 3ONA-MAST
07 98PHENTERMINE HYDROCHLORIDE
08 8PHENTERMINE HYDROCHLORIDE AND TOPIRAMATE
09 4QSYMIA
10 3SUPRENZA
11 1TORA
12 1WILPO
01 112No
02 11Yes
03 1Blank
RLD : No
TE Code : AA
Brand Name : PHENTERMINE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 37.5MG
Approval Date : 1997-05-30
Application Number : 40190
RX/OTC/DISCN : RX
RLD : No
TE Code : AA
RLD : No
TE Code :
Brand Name : PHENTERMINE HYDROCHLORIDE
Dosage Form : CAPSULE;ORAL
Dosage Strength : 30MG
Approval Date : 1997-06-18
Application Number : 40227
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Brand Name : PHENTERMINE HYDROCHLORIDE
Dosage Form : CAPSULE;ORAL
Dosage Strength : 37.5MG
Approval Date : 1997-06-19
Application Number : 40228
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Brand Name : FASTIN
Dosage Form : CAPSULE;ORAL
Dosage Strength : 30MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1982-01-01
Application Number : 17352
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : Yes
TE Code :
Brand Name : WILPO
Dosage Form : TABLET;ORAL
Dosage Strength : 8MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1982-01-01
Application Number : 12737
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : No
TE Code :
Brand Name : PHENTERMINE HYDROCHLORIDE
Dosage Form : CAPSULE;ORAL
Dosage Strength : 30MG
Approval Date : 1997-03-07
Application Number : 40083
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : Yes
TE Code : AB
PHENTERMINE HYDROCHLORIDE; TOPIRAMATE
Brand Name : QSYMIA
Dosage Form : CAPSULE, EXTENDED RELEASE;ORAL
Dosage Strength : EQ 3.75MG BASE;23MG
Approval Date : 2012-07-17
Application Number : 22580
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AB
RLD : Yes
TE Code : AB
PHENTERMINE HYDROCHLORIDE; TOPIRAMATE
Brand Name : QSYMIA
Dosage Form : CAPSULE, EXTENDED RELEASE;ORAL
Dosage Strength : EQ 7.5MG BASE;46MG
Approval Date : 2012-07-17
Application Number : 22580
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AB
RLD : Yes
TE Code : AB
PHENTERMINE HYDROCHLORIDE; TOPIRAMATE
Brand Name : QSYMIA
Dosage Form : CAPSULE, EXTENDED RELEASE;ORAL
Dosage Strength : EQ 11.25MG BASE;69MG
Approval Date : 2012-07-17
Application Number : 22580
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AB
RLD : Yes
TE Code : AB
PHENTERMINE HYDROCHLORIDE; TOPIRAMATE
Brand Name : QSYMIA
Dosage Form : CAPSULE, EXTENDED RELEASE;ORAL
Dosage Strength : EQ 15MG BASE;92MG
Approval Date : 2012-07-17
Application Number : 22580
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AB
