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Metoprolol Tartrate and Hydrochlorothiazide
Metoprolol Tartrate and Hydrochlorothiazide - 62756-369-18 - (Metoprolol Tartrate and Hydrochlorothiazide)
Drug Information of Metoprolol Tartrate and Hydrochlorothiazide
| Product NDC: | 62756-369 |
| Proprietary Name: | Metoprolol Tartrate and Hydrochlorothiazide |
| Non Proprietary Name: | Metoprolol Tartrate and Hydrochlorothiazide |
| Active Ingredient(s): | 50; 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: | 62756-369 |
| Labeler Name: | Sun Pharmaceutical Industries Limited |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA090654 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20120128 |
Package Information of Metoprolol Tartrate and Hydrochlorothiazide
| Package NDC: | 62756-369-18 |
| Package Description: | 1000 TABLET in 1 BOTTLE (62756-369-18) |
NDC Information of Metoprolol Tartrate and Hydrochlorothiazide
| NDC Code | 62756-369-18 |
| Proprietary Name | Metoprolol Tartrate and Hydrochlorothiazide |
| Package Description | 1000 TABLET in 1 BOTTLE (62756-369-18) |
| Product NDC | 62756-369 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Metoprolol Tartrate and Hydrochlorothiazide |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20120128 |
| Marketing Category Name | ANDA |
| Labeler Name | Sun Pharmaceutical Industries Limited |
| Substance Name | HYDROCHLOROTHIAZIDE; METOPROLOL TARTRATE |
| Strength Number | 50; 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] |
