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hydrochlorothiazide
hydrochlorothiazide - 16714-383-03 - (Hydrochlorothiazide)
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: | 16714-383-03 |
| Package Description: | 10 BLISTER PACK in 1 CARTON (16714-383-03) > 10 CAPSULE in 1 BLISTER PACK |
NDC Information of hydrochlorothiazide
| NDC Code | 16714-383-03 |
| Proprietary Name | hydrochlorothiazide |
| Package Description | 10 BLISTER PACK in 1 CARTON (16714-383-03) > 10 CAPSULE in 1 BLISTER PACK |
| 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] |
