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DORZOLAMIDE HYDROCHLORIDE - 61314-019-10 - (dorzolamide hydrochloride)

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Drug Information of DORZOLAMIDE HYDROCHLORIDE

Product NDC: 61314-019
Proprietary Name: DORZOLAMIDE HYDROCHLORIDE
Non Proprietary Name: dorzolamide hydrochloride
Active Ingredient(s): 20    mg/mL & nbsp;   dorzolamide hydrochloride
Administration Route(s): OPHTHALMIC
Dosage Form(s): SOLUTION/ DROPS
Coding System: National Drug Codes(NDC)

Labeler Information of DORZOLAMIDE HYDROCHLORIDE

Product NDC: 61314-019
Labeler Name: Sandoz Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078981
Marketing Category: ANDA
Start Marketing Date: 20090601

Package Information of DORZOLAMIDE HYDROCHLORIDE

Package NDC: 61314-019-10
Package Description: 10 mL in 1 BOTTLE (61314-019-10)

NDC Information of DORZOLAMIDE HYDROCHLORIDE

NDC Code 61314-019-10
Proprietary Name DORZOLAMIDE HYDROCHLORIDE
Package Description 10 mL in 1 BOTTLE (61314-019-10)
Product NDC 61314-019
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name dorzolamide hydrochloride
Dosage Form Name SOLUTION/ DROPS
Route Name OPHTHALMIC
Start Marketing Date 20090601
Marketing Category Name ANDA
Labeler Name Sandoz Inc.
Substance Name DORZOLAMIDE HYDROCHLORIDE
Strength Number 20
Strength Unit mg/mL
Pharmaceutical Classes Carbonic Anhydrase Inhibitor [EPC],Carbonic Anhydrase Inhibitors [MoA]

Complete Information of DORZOLAMIDE HYDROCHLORIDE


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