Product NDC: | 49349-721 |
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) |
Product NDC: | 49349-721 |
Labeler Name: | REMEDYREPACK INC. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA040807 |
Marketing Category: | ANDA |
Start Marketing Date: | 20110830 |
Package NDC: | 49349-721-02 |
Package Description: | 30 CAPSULE in 1 BLISTER PACK (49349-721-02) |
NDC Code | 49349-721-02 |
Proprietary Name | Hydrochlorothiazide |
Package Description | 30 CAPSULE in 1 BLISTER PACK (49349-721-02) |
Product NDC | 49349-721 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Hydrochlorothiazide |
Dosage Form Name | CAPSULE |
Route Name | ORAL |
Start Marketing Date | 20110830 |
Marketing Category Name | ANDA |
Labeler Name | REMEDYREPACK INC. |
Substance Name | HYDROCHLOROTHIAZIDE |
Strength Number | 12.5 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [Chemical/Ingredient] |