01 1ABC HOLDING
02 7Actavis Inc
03 1Aurobindo Pharma Limited
04 2Aurolife Pharma LLC
05 1Avanthi Pharma
06 3Barr Laboratories
07 2Camall
08 14Chartwell Pharmaceuticals llc
09 3Citius Pharmaceuticals
10 1DURAMED PHARMS BARR
11 8Elite Laboratories
12 1Ferndale Laboratories, Inc.
13 1GSK
14 1Hanlim Pharmaceuticals Inc
15 2IVAX Pharmaceuticals Inc
16 5InvaGen Pharmaceuticals Inc
17 6KVK.Tech
18 5Lannett Company, Inc.
19 3MAST MM
20 1Merro Pharmaceutical
21 1Myungmoon Pharm. Co., LTD.
22 1Novast Laboratories
23 4Nuvo Pharmaceuticals
24 1Prinston
25 1SHIRE PLC
26 11Sandoz B2B
27 1Solvay Chemicals International S.A
28 8Sun Pharmaceutical Industries Limited
29 1TG United
30 8Teva Pharmaceutical Industries
31 4USL PHARMA
32 2Upsher-Smith Laboratories
33 4VITARINE
34 4Vivus
35 3Zydus Pharmaceuticals
01 8CAPSULE, EXTENDED RELEASE;ORAL
02 1CAPSULE; ORAL
03 70CAPSULE;ORAL
04 2TABLET
05 6TABLET, ORALLY DISINTEGRATING;ORAL
06 35TABLET;ORAL
01 82DISCN
02 2Generic
03 37RX
04 1Blank
01 2ADIPEX-P
02 1FASTIN
03 1LOMAIRA
04 1Lediphen
05 1OBESTIN-30
06 1OBY-TRIM
07 3ONA-MAST
08 1PENTAGEN
09 98PHENTERMINE HYDROCHLORIDE
10 4PHENTERMINE HYDROCHLORIDE AND TOPIRAMATE
11 4QSYMIA
12 3SUPRENZA
13 1TORA
14 1WILPO
01 2South Korea
02 120USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : PHENTERMINE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 37.5MG
Packaging :
Approval Date : 1998-11-25
Application Number : 40276
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : PHENTERMINE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 8MG
Packaging :
Approval Date : 1982-01-01
Application Number : 83923
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : PHENTERMINE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 37.5MG
Packaging :
Approval Date : 1997-05-30
Application Number : 40190
Regulatory Info : RX
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : PHENTERMINE HYDROCHLORIDE
Dosage Form : CAPSULE;ORAL
Dosage Strength : 30MG
Packaging :
Approval Date : 1997-06-18
Application Number : 40227
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : PHENTERMINE HYDROCHLORIDE
Dosage Form : CAPSULE;ORAL
Dosage Strength : 37.5MG
Packaging :
Approval Date : 1997-06-19
Application Number : 40228
Regulatory Info : RX
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : PHENTERMINE HYDROCHLORIDE
Dosage Form : CAPSULE;ORAL
Dosage Strength : 30MG
Packaging :
Approval Date : 2003-01-22
Application Number : 40448
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : PHENTERMINE HYDROCHLORIDE
Dosage Form : CAPSULE;ORAL
Dosage Strength : 15MG
Packaging :
Approval Date : 2003-01-14
Application Number : 40460
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
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**
Packaging :
Approval Date : 1982-01-01
Application Number : 17352
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : PHENTERMINE HYDROCHLORIDE
Dosage Form : CAPSULE;ORAL
Dosage Strength : 30MG
Packaging :
Approval Date : 2008-03-21
Application Number : 40875
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : PHENTERMINE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 37.5MG
Packaging :
Approval Date : 2008-03-31
Application Number : 40876
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : PHENTERMINE HYDROCHLORIDE
Dosage Form : CAPSULE;ORAL
Dosage Strength : 30MG
Packaging :
Approval Date : 2008-03-31
Application Number : 40886
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : PHENTERMINE HYDROCHLORIDE
Dosage Form : CAPSULE;ORAL
Dosage Strength : 15MG
Packaging :
Approval Date : 2008-03-31
Application Number : 40886
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : PHENTERMINE HYDROCHLORIDE
Dosage Form : CAPSULE;ORAL
Dosage Strength : 37.5MG
Packaging :
Approval Date : 2008-04-24
Application Number : 40887
Regulatory Info : RX
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : PHENTERMINE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 37.5MG
Packaging :
Approval Date : 2005-04-15
Application Number : 40555
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : PHENTERMINE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 37.5MG
Packaging :
Approval Date : 2002-01-04
Application Number : 40377
Regulatory Info : RX
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
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**
Packaging :
Approval Date : 1982-01-01
Application Number : 12737
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : PHENTERMINE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 37.5MG
Packaging :
Approval Date : 2001-08-30
Application Number : 40402
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : PHENTERMINE HYDROCHLORIDE
Dosage Form : CAPSULE;ORAL
Dosage Strength : 30MG
Packaging :
Approval Date : 2001-08-30
Application Number : 40403
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : PHENTERMINE HYDROCHLORIDE
Dosage Form : CAPSULE;ORAL
Dosage Strength : 30MG
Packaging :
Approval Date : 2001-08-30
Application Number : 40427
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : PHENTERMINE HYDROCHLORIDE
Dosage Form : CAPSULE;ORAL
Dosage Strength : 15MG
Packaging :
Approval Date : 2003-03-13
Application Number : 40497
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : PHENTERMINE HYDROCHLORIDE
Dosage Form : CAPSULE;ORAL
Dosage Strength : 30MG
Packaging :
Approval Date : 2003-10-23
Application Number : 40525
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : PHENTERMINE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 37.5MG
Packaging :
Approval Date : 2003-10-23
Application Number : 40526
Regulatory Info : RX
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : PHENTERMINE HYDROCHLORIDE
Dosage Form : CAPSULE;ORAL
Dosage Strength : 37.5MG
Packaging :
Approval Date : 2003-10-23
Application Number : 40527
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : PHENTERMINE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 37.5MG
Packaging :
Approval Date : 2007-08-21
Application Number : 40790
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : PHENTERMINE HYDROCHLORIDE
Dosage Form : CAPSULE;ORAL
Dosage Strength : 30MG
Packaging :
Approval Date : 1997-03-07
Application Number : 40083
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : PHENTERMINE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 8MG
Packaging :
Approval Date : 1982-01-01
Application Number : 83804
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
PHENTERMINE HYDROCHLORIDE; TOPIRAMATE
Brand Name : QSYMIA
Dosage Form : CAPSULE, EXTENDED RELEASE;ORAL
Dosage Strength : EQ 3.75MG BASE;23MG
Packaging :
Approval Date : 2012-07-17
Application Number : 22580
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
PHENTERMINE HYDROCHLORIDE; TOPIRAMATE
Brand Name : QSYMIA
Dosage Form : CAPSULE, EXTENDED RELEASE;ORAL
Dosage Strength : EQ 7.5MG BASE;46MG
Packaging :
Approval Date : 2012-07-17
Application Number : 22580
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
PHENTERMINE HYDROCHLORIDE; TOPIRAMATE
Brand Name : QSYMIA
Dosage Form : CAPSULE, EXTENDED RELEASE;ORAL
Dosage Strength : EQ 11.25MG BASE;69MG
Packaging :
Approval Date : 2012-07-17
Application Number : 22580
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
PHENTERMINE HYDROCHLORIDE; TOPIRAMATE
Brand Name : QSYMIA
Dosage Form : CAPSULE, EXTENDED RELEASE;ORAL
Dosage Strength : EQ 15MG BASE;92MG
Packaging :
Approval Date : 2012-07-17
Application Number : 22580
Regulatory Info : RX
Registration Country : USA
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