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METOPROLOL TARTRATE AND HYDROCHLOROTHIAZIDE
METOPROLOL TARTRATE AND HYDROCHLOROTHIAZIDE - 54868-5524-0 - (metoprolol tartrate and hydrochlorothiazide)
Drug Information of METOPROLOL TARTRATE AND HYDROCHLOROTHIAZIDE
| Product NDC: | 54868-5524 |
| Proprietary Name: | METOPROLOL TARTRATE AND HYDROCHLOROTHIAZIDE |
| Non Proprietary Name: | metoprolol tartrate and hydrochlorothiazide |
| Active Ingredient(s): | 25; 100 mg/1; mg/1 & nbsp; metoprolol tartrate and hydrochlorothiazide |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of METOPROLOL TARTRATE AND HYDROCHLOROTHIAZIDE
| Product NDC: | 54868-5524 |
| Labeler Name: | Physicians Total Care, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA076792 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20060207 |
Package Information of METOPROLOL TARTRATE AND HYDROCHLOROTHIAZIDE
| Package NDC: | 54868-5524-0 |
| Package Description: | 30 TABLET in 1 BOTTLE, PLASTIC (54868-5524-0) |
NDC Information of METOPROLOL TARTRATE AND HYDROCHLOROTHIAZIDE
| NDC Code | 54868-5524-0 |
| Proprietary Name | METOPROLOL TARTRATE AND HYDROCHLOROTHIAZIDE |
| Package Description | 30 TABLET in 1 BOTTLE, PLASTIC (54868-5524-0) |
| Product NDC | 54868-5524 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | metoprolol tartrate and hydrochlorothiazide |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20060207 |
| Marketing Category Name | ANDA |
| Labeler Name | Physicians Total Care, Inc. |
| Substance Name | HYDROCHLOROTHIAZIDE; METOPROLOL TARTRATE |
| Strength Number | 25; 100 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes | Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC],Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [Chemical/Ingredient] |
