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 1DURAMED PHARMS BARR
13 3ELITE LABS
14 5ELITE LABS INC
15 1FERNDALE LABS
16 1GLAXOSMITHKLINE
17 5INVAGEN PHARMS
18 2IVAX PHARMS
19 5KVK TECH
20 1KVK TECH INC
21 3LANNETT
22 2LANNETT CO INC
23 3MAST MM
24 1MERRO PHARM USA
25 1NOVAST LABS
26 4NUVO PHARM
27 1PRINSTON INC
28 10SANDOZ
29 1SANDOZ INC
30 1SHIRE RICHWOOD
31 1SOLVAY
32 1SUN PHARM INDS INC
33 3SUN PHARM INDUSTRIES
34 8TEVA
35 1TG UNITED INC
36 2UPSHER SMITH LABS
37 4USL PHARMA
38 4VITARINE
39 4VIVUS LLC
40 2WATSON LABS
41 3ZYDUS PHARMS
01 8CAPSULE, EXTENDED RELEASE;ORAL
02 1CAPSULE; ORAL
03 70CAPSULE;ORAL
04 6TABLET, ORALLY DISINTEGRATING;ORAL
05 35TABLET;ORAL
01 82DISCN
02 37RX
03 1Blank
01 2ADIPEX-P
02 1FASTIN
03 1LOMAIRA
04 1OBESTIN-30
05 1OBY-TRIM
06 3ONA-MAST
07 98PHENTERMINE HYDROCHLORIDE
08 4PHENTERMINE HYDROCHLORIDE AND TOPIRAMATE
09 4QSYMIA
10 3SUPRENZA
11 1TORA
12 1WILPO
01 108No
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 : AA
Brand Name : PHENTERMINE HYDROCHLORIDE
Dosage Form : CAPSULE;ORAL
Dosage Strength : 37.5MG
Approval Date : 1997-06-19
Application Number : 40228
RX/OTC/DISCN : RX
RLD : No
TE Code : AA
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Dosage Strength : 30MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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Dosage Strength : 8MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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
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