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hydrochlorothiazide - 16714-383-01 - (Hydrochlorothiazide)

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Drug Information of hydrochlorothiazide

Product NDC: 16714-383
Proprietary Name: hydrochlorothiazide
Non Proprietary Name: Hydrochlorothiazide
Active Ingredient(s): 12.5    mg/1 & nbsp;   Hydrochlorothiazide
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of hydrochlorothiazide

Product NDC: 16714-383
Labeler Name: NorthStar RxLLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA200645
Marketing Category: ANDA
Start Marketing Date: 20101217

Package Information of hydrochlorothiazide

Package NDC: 16714-383-01
Package Description: 30 CAPSULE in 1 BOTTLE (16714-383-01)

NDC Information of hydrochlorothiazide

NDC Code 16714-383-01
Proprietary Name hydrochlorothiazide
Package Description 30 CAPSULE in 1 BOTTLE (16714-383-01)
Product NDC 16714-383
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Hydrochlorothiazide
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20101217
Marketing Category Name ANDA
Labeler Name NorthStar RxLLC
Substance Name HYDROCHLOROTHIAZIDE
Strength Number 12.5
Strength Unit mg/1
Pharmaceutical Classes Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [Chemical/Ingredient]

Complete Information of hydrochlorothiazide


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