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Microzide
Microzide - 52544-622-01 - (Hydrochlorothiazide)
Drug Information of Microzide
| Product NDC: | 52544-622 |
| Proprietary Name: | Microzide |
| Non Proprietary Name: | Hydrochlorothiazide |
| Active Ingredient(s): | 12.5 mg/1 & nbsp; Hydrochlorothiazide |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE, GELATIN COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Microzide
| Product NDC: | 52544-622 |
| Labeler Name: | Watson Pharma, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020504 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19961227 |
Package Information of Microzide
| Package NDC: | 52544-622-01 |
| Package Description: | 100 CAPSULE, GELATIN COATED in 1 BOTTLE (52544-622-01) |
NDC Information of Microzide
| NDC Code | 52544-622-01 |
| Proprietary Name | Microzide |
| Package Description | 100 CAPSULE, GELATIN COATED in 1 BOTTLE (52544-622-01) |
| Product NDC | 52544-622 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Hydrochlorothiazide |
| Dosage Form Name | CAPSULE, GELATIN COATED |
| Route Name | ORAL |
| Start Marketing Date | 19961227 |
| Marketing Category Name | NDA |
| Labeler Name | Watson Pharma, Inc. |
| Substance Name | HYDROCHLOROTHIAZIDE |
| Strength Number | 12.5 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [Chemical/Ingredient] |
