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01 2DIPHENHYDRAMINE HYDROCHLORIDE

02 1DOXYLAMINE SUCCINATE

03 3IBUPROFEN

04 1LOPERAMIDE HYDROCHLORIDE

05 1METRONIDAZOLE

06 1NAPROXEN SODIUM

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PharmaCompass

01

Brand Name : DIPHENHYDRAMINE HYDR...

Pharmtech & Ingredients
Not Confirmed
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Brand Name : DIPHENHYDRAMINE HYDR...

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Pharmtech & Ingredients
Not Confirmed

LNK

Dosage Form : CAPSULE;ORAL

Brand Name : DIPHENHYDRAMINE HYDROCHLO...

Dosage Strength : 25MG

Packaging :

Approval Date : 1983-01-27

Application Number : 87977

Regulatory Info : DISCN

Registration Country : USA

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02

Brand Name : DIPHENHYDRAMINE HYDR...

Pharmtech & Ingredients
Not Confirmed
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Brand Name : DIPHENHYDRAMINE HYDR...

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Pharmtech & Ingredients
Not Confirmed

LNK

Dosage Form : CAPSULE;ORAL

Brand Name : DIPHENHYDRAMINE HYDROCHLO...

Dosage Strength : 50MG

Packaging :

Approval Date : 1983-01-27

Application Number : 87978

Regulatory Info : DISCN

Registration Country : USA

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03

Brand Name : DOXYLAMINE SUCCINATE

Pharmtech & Ingredients
Not Confirmed
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Brand Name : DOXYLAMINE SUCCINATE

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Pharmtech & Ingredients
Not Confirmed

LNK

Dosage Form : TABLET;ORAL

Brand Name : DOXYLAMINE SUCCINATE

Dosage Strength : 25MG

Packaging :

Approval Date : 2004-08-27

Application Number : 40564

Regulatory Info : OTC

Registration Country : USA

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04

Brand Name : IBUPROFEN

Pharmtech & Ingredients
Not Confirmed
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Brand Name : IBUPROFEN

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Pharmtech & Ingredients
Not Confirmed

LNK

Dosage Form : TABLET;ORAL

Brand Name : IBUPROFEN

Dosage Strength : 200MG

Packaging :

Approval Date : 1999-03-01

Application Number : 75010

Regulatory Info : OTC

Registration Country : USA

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05

Brand Name : IBUPROFEN

Pharmtech & Ingredients
Not Confirmed
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Brand Name : IBUPROFEN

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Pharmtech & Ingredients
Not Confirmed

LNK

Dosage Form : TABLET;ORAL

Brand Name : IBUPROFEN

Dosage Strength : 200MG

Packaging :

Approval Date : 1999-03-01

Application Number : 75139

Regulatory Info : OTC

Registration Country : USA

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06

Brand Name : IBUPROFEN

Pharmtech & Ingredients
Not Confirmed
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Brand Name : IBUPROFEN

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Pharmtech & Ingredients
Not Confirmed

LNK

Dosage Form : TABLET;ORAL

Brand Name : IBUPROFEN

Dosage Strength : 100MG

Packaging :

Approval Date : 2004-06-17

Application Number : 76741

Regulatory Info : DISCN

Registration Country : USA

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07

Brand Name : LOPERAMIDE HYDROCHLO...

Pharmtech & Ingredients
Not Confirmed
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Brand Name : LOPERAMIDE HYDROCHLO...

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Pharmtech & Ingredients
Not Confirmed

LNK

Dosage Form : TABLET;ORAL

Brand Name : LOPERAMIDE HYDROCHLORIDE

Dosage Strength : 2MG

Packaging :

Approval Date : 2003-06-10

Application Number : 76497

Regulatory Info : OTC

Registration Country : USA

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08

Brand Name : METRONIDAZOLE

Pharmtech & Ingredients
Not Confirmed
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Brand Name : METRONIDAZOLE

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Pharmtech & Ingredients
Not Confirmed

LNK

Dosage Form : TABLET;ORAL

Brand Name : METRONIDAZOLE

Dosage Strength : 250MG

Packaging :

Approval Date : 1984-04-10

Application Number : 19029

Regulatory Info : DISCN

Registration Country : USA

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09

Brand Name : NAPROXEN SODIUM

Pharmtech & Ingredients
Not Confirmed
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Brand Name : NAPROXEN SODIUM

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Pharmtech & Ingredients
Not Confirmed

LNK

Dosage Form : TABLET;ORAL

Brand Name : NAPROXEN SODIUM

Dosage Strength : 220MG

Packaging :

Approval Date : 2017-01-23

Application Number : 204872

Regulatory Info : OTC

Registration Country : USA

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