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Hydroxychloroquine Sulfate - 49349-162-02 - (Hydroxychloroquine Sulfate)

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Drug Information of Hydroxychloroquine Sulfate

Product NDC: 49349-162
Proprietary Name: Hydroxychloroquine Sulfate
Non Proprietary Name: Hydroxychloroquine Sulfate
Active Ingredient(s): 200    mg/1 & nbsp;   Hydroxychloroquine Sulfate
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Hydroxychloroquine Sulfate

Product NDC: 49349-162
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040766
Marketing Category: ANDA
Start Marketing Date: 20110413

Package Information of Hydroxychloroquine Sulfate

Package NDC: 49349-162-02
Package Description: 30 TABLET in 1 BLISTER PACK (49349-162-02)

NDC Information of Hydroxychloroquine Sulfate

NDC Code 49349-162-02
Proprietary Name Hydroxychloroquine Sulfate
Package Description 30 TABLET in 1 BLISTER PACK (49349-162-02)
Product NDC 49349-162
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Hydroxychloroquine Sulfate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110413
Marketing Category Name ANDA
Labeler Name REMEDYREPACK INC.
Substance Name HYDROXYCHLOROQUINE SULFATE
Strength Number 200
Strength Unit mg/1
Pharmaceutical Classes Antirheumatic Agent [EPC]

Complete Information of Hydroxychloroquine Sulfate


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