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01 1ACYCLOVIR

02 2AMITRIPTYLINE HYDROCHLORIDE; CHLORDIAZEPOXIDE

03 1BETAMETHASONE DIPROPIONATE

04 6BREXPIPRAZOLE

05 1CALCITRIOL

06 3CEFDINIR

07 2CEFPODOXIME PROXETIL

08 1CEFTRIAXONE SODIUM

09 3CEFUROXIME AXETIL

10 2CEPHALEXIN

11 2CLOBAZAM

12 2CYCLOBENZAPRINE HYDROCHLORIDE

13 1DIATRIZOATE MEGLUMINE; DIATRIZOATE SODIUM

14 1ESOMEPRAZOLE MAGNESIUM

15 1FLUOCINOLONE ACETONIDE

16 4HYDRALAZINE HYDROCHLORIDE

17 2LEVETIRACETAM

18 3LEVOFLOXACIN

19 1LORATADINE

20 3LORAZEPAM

21 2MELOXICAM

22 2METHYLPHENIDATE HYDROCHLORIDE

23 1MOMETASONE FUROATE

24 2OMEPRAZOLE; SODIUM BICARBONATE

25 2POTASSIUM CHLORIDE

26 1PREGABALIN

27 2PRIMIDONE

28 3SERTRALINE HYDROCHLORIDE

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PharmaCompass

01

Brand Name : ACYCLOVIR

euroPLX 86 Munich
Not Confirmed
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Brand Name : ACYCLOVIR

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euroPLX 86 Munich
Not Confirmed

ANDA Repository

Dosage Form : OINTMENT;TOPICAL

Brand Name : ACYCLOVIR

Dosage Strength : 5%

Packaging :

Approval Date : 2017-07-31

Application Number : 206437

Regulatory Info : DISCN

Registration Country : USA

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02

Brand Name : CHLORDIAZEPOXIDE AND...

euroPLX 86 Munich
Not Confirmed
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Brand Name : CHLORDIAZEPOXIDE AND...

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euroPLX 86 Munich
Not Confirmed

ANDA Repository

Dosage Form : TABLET;ORAL

Brand Name : CHLORDIAZEPOXIDE AND AMIT...

Dosage Strength : EQ 12.5MG BASE;5MG

Packaging :

Approval Date : 1986-12-10

Application Number : 70765

Regulatory Info : DISCN

Registration Country : USA

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03

Brand Name : CHLORDIAZEPOXIDE AND...

euroPLX 86 Munich
Not Confirmed
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Brand Name : CHLORDIAZEPOXIDE AND...

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euroPLX 86 Munich
Not Confirmed

ANDA Repository

Dosage Form : TABLET;ORAL

Brand Name : CHLORDIAZEPOXIDE AND AMIT...

Dosage Strength : EQ 25MG BASE;10MG

Packaging :

Approval Date : 1986-12-10

Application Number : 70766

Regulatory Info : DISCN

Registration Country : USA

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04

Brand Name : BETAMETHASONE DIPROP...

euroPLX 86 Munich
Not Confirmed
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Brand Name : BETAMETHASONE DIPROP...

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euroPLX 86 Munich
Not Confirmed

ANDA Repository

Dosage Form : CREAM, AUGMENTED;TOPICAL

Brand Name : BETAMETHASONE DIPROPIONAT...

Dosage Strength : EQ 0.05% BASE

Packaging :

Approval Date : 2004-01-23

Application Number : 76603

Regulatory Info : DISCN

Registration Country : USA

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05

Brand Name : BREXPIPRAZOLE

euroPLX 86 Munich
Not Confirmed
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Brand Name : BREXPIPRAZOLE

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euroPLX 86 Munich
Not Confirmed

ANDA Repository

Dosage Form : TABLET;ORAL

Brand Name : BREXPIPRAZOLE

Dosage Strength : 0.25MG

Packaging :

Approval Date : 2023-10-25

Application Number : 213758

Regulatory Info : DISCN

Registration Country : USA

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06

Brand Name : BREXPIPRAZOLE

euroPLX 86 Munich
Not Confirmed
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Brand Name : BREXPIPRAZOLE

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euroPLX 86 Munich
Not Confirmed

ANDA Repository

Dosage Form : TABLET;ORAL

Brand Name : BREXPIPRAZOLE

Dosage Strength : 0.5MG

Packaging :

Approval Date : 2023-10-25

Application Number : 213758

Regulatory Info : DISCN

Registration Country : USA

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07

Brand Name : BREXPIPRAZOLE

euroPLX 86 Munich
Not Confirmed
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Brand Name : BREXPIPRAZOLE

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euroPLX 86 Munich
Not Confirmed

ANDA Repository

Dosage Form : TABLET;ORAL

Brand Name : BREXPIPRAZOLE

Dosage Strength : 1MG

Packaging :

Approval Date : 2023-10-25

Application Number : 213758

Regulatory Info : DISCN

Registration Country : USA

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08

Brand Name : BREXPIPRAZOLE

euroPLX 86 Munich
Not Confirmed
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Brand Name : BREXPIPRAZOLE

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euroPLX 86 Munich
Not Confirmed

ANDA Repository

Dosage Form : TABLET;ORAL

Brand Name : BREXPIPRAZOLE

Dosage Strength : 2MG

Packaging :

Approval Date : 2023-10-25

Application Number : 213758

Regulatory Info : DISCN

Registration Country : USA

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09

Brand Name : BREXPIPRAZOLE

euroPLX 86 Munich
Not Confirmed
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Brand Name : BREXPIPRAZOLE

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euroPLX 86 Munich
Not Confirmed

ANDA Repository

Dosage Form : TABLET;ORAL

Brand Name : BREXPIPRAZOLE

Dosage Strength : 3MG

Packaging :

Approval Date : 2023-10-25

Application Number : 213758

Regulatory Info : DISCN

Registration Country : USA

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10

Brand Name : BREXPIPRAZOLE

euroPLX 86 Munich
Not Confirmed
arrow

Brand Name : BREXPIPRAZOLE

arrow
euroPLX 86 Munich
Not Confirmed

ANDA Repository

Dosage Form : TABLET;ORAL

Brand Name : BREXPIPRAZOLE

Dosage Strength : 4MG

Packaging :

Approval Date : 2023-10-25

Application Number : 213758

Regulatory Info : DISCN

Registration Country : USA

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