DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
01 1DR REDDYS
02 3DR REDDYS LABS INC
03 2ALEMBIC
04 2ANTARES PHARMA INC
05 3AUROBINDO PHARMA
06 1AUROBINDO PHARMA LTD
07 1BAXTER HLTHCARE CORP
08 1CAPLIN
09 3CHARTWELL MOLECULAR
10 1CIPLA
11 3CURRAX
12 1DR REDDYS LABS LTD
13 2ENDO OPERATIONS
14 1EUGIA PHARMA
15 3FOSUN PHARMA
16 3FRESENIUS KABI USA
17 9GLAXOSMITHKLINE
18 2HIKMA
19 3HIKMA PHARMS
20 3IPCA LABS LTD
21 2LANNETT CO INC
22 1MERIDIAN MEDCL
23 6MYLAN
24 1NORVIUM BIOSCIENCE
25 3ONESOURCE SPECIALTY
26 3ORBION PHARMS
27 2PADAGIS ISRAEL
28 1PAR PHARM
29 1PERRIGO UK FINCO
30 2PH HEALTH
31 1REGCON HOLDINGS
32 1RISING
33 3ROXANE
34 2SANDOZ
35 2SUN PHARM
36 3SUN PHARM INDS
37 3SUN PHARM INDS LTD
38 3TEVA
39 1TEVA BRANDED PHARM
40 2TEVA PARENTERAL
41 1TEVA PHARMS USA
42 2TONIX MEDS
43 3VKT PHARMA
44 3WATSON LABS
45 1WOCKHARDT BIO AG
46 3ZHEJIANG
47 1ZYDUS
01 33INJECTABLE;SUBCUTANEOUS
02 1POWDER;NASAL
03 1SOLUTION;SUBCUTANEOUS
04 11SPRAY;NASAL
05 1SYSTEM;IONTOPHORESIS
06 5TABLET; ORAL
07 53TABLET;ORAL
01 44DISCN
02 55RX
03 6Blank
01 1ALSUMA
02 7IMITREX
03 2IMITREX STATDOSE
04 1ONZETRA XSAIL
05 7SUMATRIPTAN
06 3SUMATRIPTAN AND NAPROXEN SODIUM
07 75SUMATRIPTAN SUCCINATE
08 2SUMATRIPTAN; NAPROXEN SODIUM
09 2SUMAVEL DOSEPRO
10 1TOSYMRA
11 2TREXIMET
12 1ZECUITY
13 1ZEMBRACE SYMTOUCH
01 83No
02 16Yes
03 6Blank
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
RLD : No
TE Code : AB
Brand Name : SUMATRIPTAN SUCCINATE
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 25MG BASE
Approval Date : 2009-08-10
Application Number : 76847
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
RLD : No
TE Code : AB
Brand Name : SUMATRIPTAN SUCCINATE
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 50MG BASE
Approval Date : 2009-08-10
Application Number : 76847
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
RLD : No
TE Code : AB
Brand Name : SUMATRIPTAN SUCCINATE
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 100MG BASE
Approval Date : 2009-08-10
Application Number : 76847
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
RLD : No
TE Code : AB
Brand Name : SUMATRIPTAN SUCCINATE
Dosage Form : INJECTABLE;SUBCUTANEOUS
Dosage Strength : EQ 6MG BASE/0.5ML (EQ 12MG BASE/ML)
Approval Date : 2014-01-29
Application Number : 90495
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : Yes
TE Code :
Brand Name : IMITREX
Dosage Form : INJECTABLE;SUBCUTANEOUS
Dosage Strength : EQ 6MG BASE/0.5ML (EQ 12MG BASE/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1992-12-28
Application Number : 20080
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code : AB
Brand Name : IMITREX STATDOSE
Dosage Form : INJECTABLE;SUBCUTANEOUS
Dosage Strength : EQ 4MG BASE/0.5ML (EQ 8MG BASE/ML)
Approval Date : 2006-02-01
Application Number : 20080
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AB
RLD : Yes
TE Code : AB
Brand Name : IMITREX STATDOSE
Dosage Form : INJECTABLE;SUBCUTANEOUS
Dosage Strength : EQ 6MG BASE/0.5ML (EQ 12MG BASE/ML)
Approval Date : 1996-12-23
Application Number : 20080
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AB
RLD : Yes
TE Code : AB
Brand Name : IMITREX
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 100MG BASE
Approval Date : 1995-06-01
Application Number : 20132
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AB
RLD : Yes
TE Code : AB
Brand Name : IMITREX
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 25MG BASE
Approval Date : 1995-06-01
Application Number : 20132
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AB
RLD : Yes
TE Code : AB
Brand Name : IMITREX
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 50MG BASE
Approval Date : 1995-06-01
Application Number : 20132
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AB
