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01 3ACARBOSE

02 1ACETYLCYSTEINE

03 4ATROPINE SULFATE

04 1AZELASTINE HYDROCHLORIDE

05 1BEPOTASTINE BESILATE

06 1BIMATOPROST

07 2BRIMONIDINE TARTRATE

08 1BRIMONIDINE TARTRATE; TIMOLOL MALEATE

09 2BUPIVACAINE HYDROCHLORIDE

10 2CALCIUM GLUCONATE

11 3CISATRACURIUM BESYLATE

12 1CLONIDINE HYDROCHLORIDE

13 1CUPRIC CHLORIDE

14 2CYANOCOBALAMIN

15 3DEXAMETHASONE SODIUM PHOSPHATE

16 2DEXMEDETOMIDINE HYDROCHLORIDE

17 1DORZOLAMIDE HYDROCHLORIDE; TIMOLOL MALEATE

18 4DOXYCYCLINE

19 3DROXIDOPA

20 1EPINASTINE HYDROCHLORIDE

21 1GLYCOPYRROLATE

22 2HALOPERIDOL DECANOATE

23 1ISOPROTERENOL HYDROCHLORIDE

24 1ISOSULFAN BLUE

25 1LACOSAMIDE

26 1LATANOPROST

27 1METHOCARBAMOL

28 4NALBUPHINE HYDROCHLORIDE

29 2NALOXONE HYDROCHLORIDE

30 2OFLOXACIN

31 1OLOPATADINE HYDROCHLORIDE

32 3PILOCARPINE HYDROCHLORIDE

33 1POLYMYXIN B SULFATE; TRIMETHOPRIM SULFATE

34 2POTASSIUM PHOSPHATE, DIBASIC; POTASSIUM PHOSPHATE, MONOBASIC

35 1PROCHLORPERAZINE EDISYLATE

36 1PROPARACAINE HYDROCHLORIDE

37 7ROPIVACAINE HYDROCHLORIDE

38 6SELEGILINE

39 1SILDENAFIL CITRATE

40 1SODIUM NITROPRUSSIDE

41 1SUCCINYLCHOLINE CHLORIDE

42 1SULFAMETHOXAZOLE; TRIMETHOPRIM

43 1TIMOLOL

44 5TIMOLOL MALEATE

45 2TIZANIDINE HYDROCHLORIDE

46 1TOBRAMYCIN

47 1TRAVOPROST

48 1TROPICAMIDE

49 1VALGANCICLOVIR HYDROCHLORIDE

50 4VERAPAMIL HYDROCHLORIDE

51 1ZINC CHLORIDE

52 2ZINC SULFATE

53 2ZOLMITRIPTAN

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PharmaCompass

01

Brand Name : ACARBOSE

Fi Europe 2024
Not Confirmed
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Brand Name : ACARBOSE

Fi Europe 2024
Not Confirmed
arrow

Somerset Pharmaceuticals Inc

Dosage Form : TABLET; ORAL

Proprietary Name : ACARBOSE

Dosage Strength : 25MG

Approval Date : 2013-10-17

Application Number : 91343

RX/OTC/DISCN : RX

RLD : No

TE Code : AB

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02

Brand Name : ACARBOSE

Fi Europe 2024
Not Confirmed
arrow

Brand Name : ACARBOSE

Fi Europe 2024
Not Confirmed
arrow

Somerset Pharmaceuticals Inc

Dosage Form : TABLET; ORAL

Proprietary Name : ACARBOSE

Dosage Strength : 50MG

Approval Date : 2013-10-17

Application Number : 91343

RX/OTC/DISCN : RX

RLD : No

TE Code : AB

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03

Brand Name : ACARBOSE

Fi Europe 2024
Not Confirmed
arrow

Brand Name : ACARBOSE

Fi Europe 2024
Not Confirmed
arrow

Somerset Pharmaceuticals Inc

Dosage Form : TABLET; ORAL

Proprietary Name : ACARBOSE

Dosage Strength : 100MG

Approval Date : 2013-10-17

Application Number : 91343

RX/OTC/DISCN : RX

RLD : No

TE Code : AB

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04

Brand Name : ACETYLCYSTEINE

Fi Europe 2024
Not Confirmed
arrow

Brand Name : ACETYLCYSTEINE

Fi Europe 2024
Not Confirmed
arrow

Somerset Pharmaceuticals Inc

Dosage Form : INJECTABLE; INTRAVENOUS

Proprietary Name : ACETYLCYSTEINE

Dosage Strength : 6GM/30ML (200MG/ML)

Approval Date : 2024-06-07

Application Number : 218397

RX/OTC/DISCN : RX

RLD : No

TE Code : AP

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05

Brand Name : ATROPINE SULFATE

Fi Europe 2024
Not Confirmed
arrow

Brand Name : ATROPINE SULFATE

Fi Europe 2024
Not Confirmed
arrow

Somerset Pharmaceuticals Inc

Dosage Form : SOLUTION/DROPS; OPHTHALMIC

Proprietary Name : ATROPINE SULFATE

Dosage Strength : 1%

Approval Date : 2024-07-01

Application Number : 215618

RX/OTC/DISCN : RX

RLD : No

TE Code : AT1

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06

Brand Name : ATROPINE SULFATE

Fi Europe 2024
Not Confirmed
arrow

Brand Name : ATROPINE SULFATE

Fi Europe 2024
Not Confirmed
arrow

Somerset Pharmaceuticals Inc

Dosage Form : SOLUTION; INTRAVENOUS

Proprietary Name : ATROPINE SULFATE

Dosage Strength : 0.4MG/ML (0.4MG/ML)

Approval Date : 2024-07-03

Application Number : 215969

RX/OTC/DISCN : RX

RLD : No

TE Code : AP

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07

Brand Name : ATROPINE SULFATE

Fi Europe 2024
Not Confirmed
arrow

Brand Name : ATROPINE SULFATE

Fi Europe 2024
Not Confirmed
arrow

Somerset Pharmaceuticals Inc

Dosage Form : SOLUTION; INTRAVENOUS

Proprietary Name : ATROPINE SULFATE

Dosage Strength : 1MG/ML (1MG/ML)

Approval Date : 2024-07-03

Application Number : 215969

RX/OTC/DISCN : RX

RLD : No

TE Code : AP

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08

Brand Name : ATROPINE SULFATE

Fi Europe 2024
Not Confirmed
arrow

Brand Name : ATROPINE SULFATE

Fi Europe 2024
Not Confirmed
arrow

Somerset Pharmaceuticals Inc

Dosage Form : SOLUTION/DROPS; OPHTHALMIC

Proprietary Name : ATROPINE SULFATE

Dosage Strength : 1%

Approval Date : 2024-04-29

Application Number : 217791

RX/OTC/DISCN : RX

RLD : No

TE Code : AT2

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09

Brand Name : AZELASTINE HYDROCHLO...

Fi Europe 2024
Not Confirmed
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Brand Name : AZELASTINE HYDROCHLO...

Fi Europe 2024
Not Confirmed
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Somerset Pharmaceuticals Inc

Dosage Form : SOLUTION/DROPS; OPHTHALMIC

Proprietary Name : AZELASTINE HYDROCHLORIDE

Dosage Strength : 0.05%

Approval Date : 2019-03-29

Application Number : 207411

RX/OTC/DISCN : RX

RLD : No

TE Code : AT

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10

Brand Name : BEPOTASTINE BESILATE

Fi Europe 2024
Not Confirmed
arrow

Brand Name : BEPOTASTINE BESILATE

Fi Europe 2024
Not Confirmed
arrow

Somerset Pharmaceuticals Inc

Dosage Form : SOLUTION/DROPS; OPHTHALMIC

Proprietary Name : BEPOTASTINE BESILATE

Dosage Strength : 1.5%

Approval Date : 2024-08-14

Application Number : 217770

RX/OTC/DISCN : RX

RLD : No

TE Code : AT

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