Delivering quality and niche Active Pharmaceutical Ingredients across the global from our USFDA-approved facility.
01 3MANKIND PHARMA
02 9AMNEAL
03 3ANDAS 5 HOLDING
04 1ANI PHARMS
05 3APPCO
06 2AUROBINDO PHARMA LTD
07 1AZURITY
08 3BEXIMCO PHARMS USA
09 2ENDO OPERATIONS
10 3GRAVITI PHARMS
11 2HERITAGE
12 3HIBROW HLTHCARE
13 3IMPAX
14 2IVAX SUB TEVA PHARMS
15 3LANNETT CO INC
16 4MAIA PHARMS INC
17 2METACEL PHARMS LLC
18 3MICRO LABS
19 3NORTHSTAR HLTHCARE
20 2NOVARTIS
21 2OXFORD PHARMS
22 6PHARMOBEDIENT
23 4PIRAMAL CRITICAL
24 3RISING
25 9RUBICON RESEARCH
26 2SUN PHARM INDS INC
27 2TEVA
28 2UCB INC
29 3UNICHEM
30 2USL PHARMA
31 6WATSON LABS
32 2YILING
33 4ZYDUS LIFESCIENCES
34 1Blank
01 3GRANULES;ORAL
02 22INJECTABLE;INTRATHECAL
03 4SOLUTION;ORAL
04 2SUSPENSION;ORAL
05 2TABLET, ORALLY DISINTEGRATING;ORAL
06 72TABLET;ORAL
01 29DISCN
02 73RX
03 3Blank
01 88BACLOFEN
02 1FLEQSUVY
03 4GABLOFEN
04 2KEMSTRO
05 5LIORESAL
06 3LYVISPAH
07 1OZOBAX
08 1OZOBAX DS
01 85No
02 17Yes
03 3Blank
Delivering quality and niche Active Pharmaceutical Ingredients across the global from our USFDA-approved facility.
RLD : No
TE Code : AB
Brand Name : BACLOFEN
Dosage Form : TABLET;ORAL
Dosage Strength : 5MG
Approval Date : 2022-01-25
Application Number : 215885
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
Delivering quality and niche Active Pharmaceutical Ingredients across the global from our USFDA-approved facility.
RLD : No
TE Code : AB
Brand Name : BACLOFEN
Dosage Form : TABLET;ORAL
Dosage Strength : 10MG
Approval Date : 2022-01-25
Application Number : 215885
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
Delivering quality and niche Active Pharmaceutical Ingredients across the global from our USFDA-approved facility.
RLD : No
TE Code : AB
Brand Name : BACLOFEN
Dosage Form : TABLET;ORAL
Dosage Strength : 20MG
Approval Date : 2022-01-25
Application Number : 215885
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : Yes
TE Code : AP
Brand Name : LIORESAL
Dosage Form : INJECTABLE;INTRATHECAL
Dosage Strength : 0.5MG/ML
Approval Date : 1992-06-17
Application Number : 20075
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AP
RLD : Yes
TE Code : AP
Brand Name : LIORESAL
Dosage Form : INJECTABLE;INTRATHECAL
Dosage Strength : 2MG/ML
Approval Date : 1992-06-17
Application Number : 20075
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AP
RLD : Yes
TE Code : AP
Brand Name : LIORESAL
Dosage Form : INJECTABLE;INTRATHECAL
Dosage Strength : 0.05MG/ML
Approval Date : 1996-11-07
Application Number : 20075
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AP
RLD : Yes
TE Code :
Brand Name : LIORESAL
Dosage Form : TABLET;ORAL
Dosage Strength : 10MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1982-01-01
Application Number : 17851
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Brand Name : LIORESAL
Dosage Form : TABLET;ORAL
Dosage Strength : 20MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1982-01-20
Application Number : 17851
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Brand Name : KEMSTRO
Dosage Form : TABLET, ORALLY DISINTEGRATING;ORAL
Dosage Strength : 10MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 2003-10-30
Application Number : 21589
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Brand Name : KEMSTRO
Dosage Form : TABLET, ORALLY DISINTEGRATING;ORAL
Dosage Strength : 20MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 2003-10-30
Application Number : 21589
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
