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01 2ACETAMINOPHEN; BUTALBITAL

02 1CAFFEINE; ERGOTAMINE TARTRATE

03 1CALCITRIOL

04 3CEFDINIR

05 2CEFPODOXIME PROXETIL

06 1CEFTRIAXONE SODIUM

07 3CEFUROXIME AXETIL

08 2CEPHALEXIN

09 3CHLORZOXAZONE

10 1DIATRIZOATE MEGLUMINE; DIATRIZOATE SODIUM

11 1FLUOCINOLONE ACETONIDE

12 2LEVETIRACETAM

13 1LORATADINE

14 2METHAZOLAMIDE

15 2METHYLPHENIDATE HYDROCHLORIDE

16 6MORPHINE SULFATE

17 2OMEPRAZOLE; SODIUM BICARBONATE

18 3POTASSIUM CHLORIDE

19 1PREGABALIN

20 4PROPRANOLOL HYDROCHLORIDE

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PharmaCompass

01

Brand Name : BUTAPAP

BePharma
Not Confirmed
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Brand Name : BUTAPAP

BePharma
Not Confirmed
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ANDA Repository

Dosage Form : TABLET; ORAL

Proprietary Name : BUTAPAP

Dosage Strength : 325MG;50MG

Approval Date : 1992-10-26

Application Number : 89987

RX/OTC/DISCN : RX

RLD : No

TE Code : AA

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02

Brand Name : BUTALBITAL AND ACETA...

BePharma
Not Confirmed
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Brand Name : BUTALBITAL AND ACETA...

BePharma
Not Confirmed
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ANDA Repository

Dosage Form : TABLET; ORAL

Proprietary Name : BUTALBITAL AND ACETAMINO...

Dosage Strength : 300MG;50MG

Approval Date : 2016-11-15

Application Number : 207386

RX/OTC/DISCN : RX

RLD : No

TE Code : AA

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03

Brand Name : ERGOTAMINE TARTRATE ...

BePharma
Not Confirmed
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Brand Name : ERGOTAMINE TARTRATE ...

BePharma
Not Confirmed
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ANDA Repository

Dosage Form : TABLET; ORAL

Proprietary Name : ERGOTAMINE TARTRATE AND ...

Dosage Strength : 100MG;1MG

Approval Date : 2005-09-16

Application Number : 40590

RX/OTC/DISCN : RX

RLD : No

TE Code :

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04

Brand Name : CALCITRIOL

BePharma
Not Confirmed
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Brand Name : CALCITRIOL

BePharma
Not Confirmed
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ANDA Repository

Dosage Form : SOLUTION; ORAL

Proprietary Name : CALCITRIOL

Dosage Strength : 1MCG/ML

Approval Date : 2023-07-28

Application Number : 203973

RX/OTC/DISCN : RX

RLD : No

TE Code : AA

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05

Brand Name : CEFDINIR

BePharma
Not Confirmed
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Brand Name : CEFDINIR

BePharma
Not Confirmed
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ANDA Repository

Dosage Form : CAPSULE; ORAL

Proprietary Name : CEFDINIR

Dosage Strength : 300MG

Approval Date : 2007-07-18

Application Number : 65418

RX/OTC/DISCN : RX

RLD : No

TE Code : AB

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06

Brand Name : CEFDINIR

BePharma
Not Confirmed
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Brand Name : CEFDINIR

BePharma
Not Confirmed
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ANDA Repository

Dosage Form : FOR SUSPENSION; ORAL

Proprietary Name : CEFDINIR

Dosage Strength : 125MG/5ML

Approval Date : 2007-07-18

Application Number : 65429

RX/OTC/DISCN : RX

RLD : No

TE Code : AB

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07

Brand Name : CEFDINIR

BePharma
Not Confirmed
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Brand Name : CEFDINIR

BePharma
Not Confirmed
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ANDA Repository

Dosage Form : FOR SUSPENSION; ORAL

Proprietary Name : CEFDINIR

Dosage Strength : 250MG/5ML

Approval Date : 2007-07-18

Application Number : 65429

RX/OTC/DISCN : RX

RLD : No

TE Code : AB

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08

Brand Name : CEFPODOXIME PROXETIL

BePharma
Not Confirmed
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Brand Name : CEFPODOXIME PROXETIL

BePharma
Not Confirmed
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ANDA Repository

Dosage Form : TABLET; ORAL

Proprietary Name : CEFPODOXIME PROXETIL

Dosage Strength : EQ 100MG BASE

Approval Date : 2007-11-14

Application Number : 65388

RX/OTC/DISCN : RX

RLD : No

TE Code : AB

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09

Brand Name : CEFPODOXIME PROXETIL

BePharma
Not Confirmed
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Brand Name : CEFPODOXIME PROXETIL

BePharma
Not Confirmed
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ANDA Repository

Dosage Form : TABLET; ORAL

Proprietary Name : CEFPODOXIME PROXETIL

Dosage Strength : EQ 200MG BASE

Approval Date : 2007-11-14

Application Number : 65388

RX/OTC/DISCN : RX

RLD : No

TE Code : AB

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10

Brand Name : CEFTRIAXONE SODIUM

BePharma
Not Confirmed
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Brand Name : CEFTRIAXONE SODIUM

BePharma
Not Confirmed
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ANDA Repository

Dosage Form : INJECTABLE; INJECTION

Proprietary Name : CEFTRIAXONE SODIUM

Dosage Strength : EQ 10GM BASE/VIAL

Approval Date : 2017-01-20

Application Number : 91117

RX/OTC/DISCN : RX

RLD : No

TE Code : AP

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