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bisoprolol fumarate and hydrochlorothiazide
bisoprolol fumarate and hydrochlorothiazide - 29300-187-13 - (bisoprolol fumarate and hydrochlorothiazide)
Drug Information of bisoprolol fumarate and hydrochlorothiazide
| Product NDC: | 29300-187 |
| Proprietary Name: | bisoprolol fumarate and hydrochlorothiazide |
| Non Proprietary Name: | bisoprolol fumarate and hydrochlorothiazide |
| Active Ingredient(s): | 2.5; 6.25 mg/1; mg/1 & nbsp; bisoprolol fumarate and hydrochlorothiazide |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of bisoprolol fumarate and hydrochlorothiazide
| Product NDC: | 29300-187 |
| Labeler Name: | Unichem Pharmaceuticals (USA), Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA079106 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20101012 |
Package Information of bisoprolol fumarate and hydrochlorothiazide
| Package NDC: | 29300-187-13 |
| Package Description: | 30 TABLET in 1 BOTTLE, PLASTIC (29300-187-13) |
NDC Information of bisoprolol fumarate and hydrochlorothiazide
| NDC Code | 29300-187-13 |
| Proprietary Name | bisoprolol fumarate and hydrochlorothiazide |
| Package Description | 30 TABLET in 1 BOTTLE, PLASTIC (29300-187-13) |
| Product NDC | 29300-187 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | bisoprolol fumarate and hydrochlorothiazide |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20101012 |
| Marketing Category Name | ANDA |
| Labeler Name | Unichem Pharmaceuticals (USA), Inc. |
| Substance Name | BISOPROLOL FUMARATE; HYDROCHLOROTHIAZIDE |
| Strength Number | 2.5; 6.25 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes | Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [Chemical/Ingredient],Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC] |
