01 1ABBVIE
02 2DR REDDYS
03 2MANKIND PHARMA
04 1AKORN INC
05 1ALCON
06 4ALEMBIC
07 3AMNEAL
08 2AMRING PHARMS
09 3ANI PHARMS
10 2APOTEX
11 2APOTEX INC
12 10BAUSCH AND LOMB
13 2CAPLIN
14 1CHARTWELL MOLECULAR
15 3CHARTWELL RX
16 7EPIC PHARMA LLC
17 3EUGIA PHARMA
18 3FDC LTD
19 2FOUGERA
20 3GLAND
21 1GLENMARK PHARMS LTD
22 2HIKMA
23 3INGENUS PHARMS LLC
24 4MERCK
25 5MICRO LABS
26 3MYLAN
27 1NEW HEIGHTSRX
28 2PACIFIC PHARMA
29 1PHARMOBEDIENT
30 3QUANTUM PHARMICS
31 2REGCON HOLDINGS
32 3RISING
33 1RUBICON RESEARCH
34 7SANDOZ
35 1SENTISS
36 1SENTISS PHARMA
37 5SOMERSET
38 3SOMERSET THERAPS LLC
39 3TEVA
40 1TEVA PHARMS
41 4THEA PHARMA
42 1UPSHER SMITH LABS
43 3USL PHARMA
44 3WATSON LABS
45 1ZAMBON SPA
01 15SOLUTION, GEL FORMING/DROPS;OPHTHALMIC
02 76SOLUTION/DROPS;OPHTHALMIC
03 1SOLUTION; OPHTHALMIC
04 1SOLUTION;OPHTHALMIC
05 28TABLET;ORAL
01 47DISCN
02 72RX
03 2Blank
01 2BETIMOL
02 3BLOCADREN
03 10BRIMONIDINE TARTRATE AND TIMOLOL MALEATE
04 1BRIMONIDINE TARTRATE; TIMOLOL MALEATE
05 1COMBIGAN
06 1COSOPT
07 1COSOPT PF
08 20DORZOLAMIDE HYDROCHLORIDE AND TIMOLOL MALEATE
09 1ISTALOL
10 1TIMOLIDE 10-25
11 3TIMOLOL
12 71TIMOLOL MALEATE
13 2TIMOPTIC
14 2TIMOPTIC IN OCUDOSE
15 2TIMOPTIC-XE
01 102No
02 17Yes
03 2Blank
RLD : Yes
TE Code : AB
BRIMONIDINE TARTRATE; TIMOLOL MALEATE
Brand Name : COMBIGAN
Dosage Form : SOLUTION/DROPS;OPHTHALMIC
Dosage Strength : 0.2%;EQ 0.5% BASE
Approval Date : 2007-10-30
Application Number : 21398
RX/OTC/DISCN : RX
RLD : Yes
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 : TIMOLOL MALEATE
Dosage Form : SOLUTION, GEL FORMING/DROPS;OPHTHALMIC
Dosage Strength : EQ 0.25% BASE
Approval Date : 2022-09-22
Application Number : 215733
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 : AT1
Brand Name : TIMOLOL MALEATE
Dosage Form : SOLUTION/DROPS;OPHTHALMIC
Dosage Strength : EQ 0.25% BASE
Approval Date : 2009-09-28
Application Number : 78771
RX/OTC/DISCN : RX
RLD : No
TE Code : AT1
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
RLD : No
TE Code : AB
Brand Name : TIMOLOL MALEATE
Dosage Form : SOLUTION, GEL FORMING/DROPS;OPHTHALMIC
Dosage Strength : EQ 0.5% BASE
Approval Date : 2022-09-22
Application Number : 215733
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 : AT1
Brand Name : TIMOLOL MALEATE
Dosage Form : SOLUTION/DROPS;OPHTHALMIC
Dosage Strength : EQ 0.5% BASE
Approval Date : 2009-09-28
Application Number : 78771
RX/OTC/DISCN : RX
RLD : No
TE Code : AT1
RLD : Yes
TE Code : AT1
Brand Name : TIMOPTIC
Dosage Form : SOLUTION/DROPS;OPHTHALMIC
Dosage Strength : EQ 0.25% BASE
Approval Date : 1982-01-01
Application Number : 18086
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AT1
RLD : Yes
TE Code :
Brand Name : BLOCADREN
Dosage Form : TABLET;ORAL
Dosage Strength : 5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1982-01-01
Application Number : 18017
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Brand Name : BLOCADREN
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 : 18017
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Brand Name : BLOCADREN
Dosage Form : TABLET;ORAL
Dosage Strength : 20MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1982-01-01
Application Number : 18017
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : No
TE Code :
HYDROCHLOROTHIAZIDE; TIMOLOL MALEATE
Brand Name : TIMOLIDE 10-25
Dosage Form : TABLET;ORAL
Dosage Strength : 25MG;10MG
Approval Date : 1982-01-01
Application Number : 18061
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
