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01 2AMITRIPTYLINE HYDROCHLORIDE; CHLORDIAZEPOXIDE

02 1CALCITRIOL

03 3CEFDINIR

04 2CEFPODOXIME PROXETIL

05 1CEFTRIAXONE SODIUM

06 3CEFUROXIME AXETIL

07 2CEPHALEXIN

08 2CYCLOBENZAPRINE HYDROCHLORIDE

09 1DIATRIZOATE MEGLUMINE; DIATRIZOATE SODIUM

10 1FLUOCINOLONE ACETONIDE

11 4HYDRALAZINE HYDROCHLORIDE

12 2LEVETIRACETAM

13 1LORATADINE

14 3LORAZEPAM

15 2MELOXICAM

16 2METHYLPHENIDATE HYDROCHLORIDE

17 2OMEPRAZOLE; SODIUM BICARBONATE

18 3POTASSIUM CHLORIDE

19 1PREGABALIN

20 2PRIMIDONE

21 3SERTRALINE HYDROCHLORIDE

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PharmaCompass

01

Brand Name : CHLORDIAZEPOXIDE AND...

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Not Confirmed
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Brand Name : CHLORDIAZEPOXIDE AND...

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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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02

Brand Name : CHLORDIAZEPOXIDE AND...

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Not Confirmed
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Brand Name : CHLORDIAZEPOXIDE AND...

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PREP
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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03

Brand Name : CALCITRIOL

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Not Confirmed
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Brand Name : CALCITRIOL

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Not Confirmed

ANDA Repository

Dosage Form : SOLUTION;ORAL

Brand Name : CALCITRIOL

Dosage Strength : 1MCG/ML

Packaging :

Approval Date : 2023-07-28

Application Number : 203973

Regulatory Info : RX

Registration Country : USA

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04

Brand Name : CEFDINIR

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Not Confirmed
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Brand Name : CEFDINIR

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Not Confirmed

ANDA Repository

Dosage Form : CAPSULE;ORAL

Brand Name : CEFDINIR

Dosage Strength : 300MG

Packaging :

Approval Date : 2007-07-18

Application Number : 65418

Regulatory Info : RX

Registration Country : USA

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05

Brand Name : CEFDINIR

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Not Confirmed
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Brand Name : CEFDINIR

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Not Confirmed

ANDA Repository

Dosage Form : FOR SUSPENSION;ORAL

Brand Name : CEFDINIR

Dosage Strength : 125MG/5ML

Packaging :

Approval Date : 2007-07-18

Application Number : 65429

Regulatory Info : RX

Registration Country : USA

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06

Brand Name : CEFDINIR

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Not Confirmed
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Brand Name : CEFDINIR

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Not Confirmed

ANDA Repository

Dosage Form : FOR SUSPENSION;ORAL

Brand Name : CEFDINIR

Dosage Strength : 250MG/5ML

Packaging :

Approval Date : 2007-07-18

Application Number : 65429

Regulatory Info : RX

Registration Country : USA

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07

Brand Name : CEFPODOXIME PROXETIL

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Not Confirmed
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Brand Name : CEFPODOXIME PROXETIL

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Not Confirmed

ANDA Repository

Dosage Form : TABLET;ORAL

Brand Name : CEFPODOXIME PROXETIL

Dosage Strength : EQ 100MG BASE

Packaging :

Approval Date : 2007-11-14

Application Number : 65388

Regulatory Info : RX

Registration Country : USA

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08

Brand Name : CEFPODOXIME PROXETIL

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Not Confirmed
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Brand Name : CEFPODOXIME PROXETIL

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Not Confirmed

ANDA Repository

Dosage Form : TABLET;ORAL

Brand Name : CEFPODOXIME PROXETIL

Dosage Strength : EQ 200MG BASE

Packaging :

Approval Date : 2007-11-14

Application Number : 65388

Regulatory Info : RX

Registration Country : USA

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09

Brand Name : CEFTRIAXONE SODIUM

PackExpo
Not Confirmed
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Brand Name : CEFTRIAXONE SODIUM

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PackExpo
Not Confirmed

ANDA Repository

Dosage Form : INJECTABLE;INJECTION

Brand Name : CEFTRIAXONE SODIUM

Dosage Strength : EQ 10GM BASE/VIAL

Packaging :

Approval Date : 2017-01-20

Application Number : 91117

Regulatory Info : RX

Registration Country : USA

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10

Brand Name : CEFUROXIME AXETIL

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Not Confirmed
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Brand Name : CEFUROXIME AXETIL

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Not Confirmed

ANDA Repository

Dosage Form : TABLET;ORAL

Brand Name : CEFUROXIME AXETIL

Dosage Strength : EQ 125MG BASE

Packaging :

Approval Date : 2008-02-15

Application Number : 65359

Regulatory Info : RX

Registration Country : USA

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