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HYDROCHLOROTHIAZIDE
HYDROCHLOROTHIAZIDE - 12634-471-91 - (HYDROCHLOROTHIAZIDE)
Drug Information of HYDROCHLOROTHIAZIDE
| Product NDC: | 12634-471 |
| Proprietary Name: | HYDROCHLOROTHIAZIDE |
| Non Proprietary Name: | HYDROCHLOROTHIAZIDE |
| Active Ingredient(s): | 50 mg/1 & nbsp; HYDROCHLOROTHIAZIDE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of HYDROCHLOROTHIAZIDE
| Product NDC: | 12634-471 |
| Labeler Name: | Apotheca, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA084324 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20090630 |
Package Information of HYDROCHLOROTHIAZIDE
| Package NDC: | 12634-471-91 |
| Package Description: | 1 TABLET in 1 BLISTER PACK (12634-471-91) |
NDC Information of HYDROCHLOROTHIAZIDE
| NDC Code | 12634-471-91 |
| Proprietary Name | HYDROCHLOROTHIAZIDE |
| Package Description | 1 TABLET in 1 BLISTER PACK (12634-471-91) |
| Product NDC | 12634-471 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | HYDROCHLOROTHIAZIDE |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20090630 |
| Marketing Category Name | ANDA |
| Labeler Name | Apotheca, Inc. |
| Substance Name | HYDROCHLOROTHIAZIDE |
| Strength Number | 50 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [Chemical/Ingredient] |
