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Labetalol hydrochloride
Labetalol hydrochloride - 68084-456-01 - (Labetalol hydrochloride)
Drug Information of Labetalol hydrochloride
| Product NDC: | 68084-456 |
| Proprietary Name: | Labetalol hydrochloride |
| Non Proprietary Name: | Labetalol hydrochloride |
| Active Ingredient(s): | 200 mg/1 & nbsp; Labetalol hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Labetalol hydrochloride
| Product NDC: | 68084-456 |
| Labeler Name: | American Health Packaging |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA075133 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20110211 |
Package Information of Labetalol hydrochloride
| Package NDC: | 68084-456-01 |
| Package Description: | 10 BLISTER PACK in 1 CARTON (68084-456-01) > 10 TABLET, FILM COATED in 1 BLISTER PACK (68084-456-11) |
NDC Information of Labetalol hydrochloride
| NDC Code | 68084-456-01 |
| Proprietary Name | Labetalol hydrochloride |
| Package Description | 10 BLISTER PACK in 1 CARTON (68084-456-01) > 10 TABLET, FILM COATED in 1 BLISTER PACK (68084-456-11) |
| Product NDC | 68084-456 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Labetalol hydrochloride |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20110211 |
| Marketing Category Name | ANDA |
| Labeler Name | American Health Packaging |
| Substance Name | LABETALOL HYDROCHLORIDE |
| Strength Number | 200 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC] |
