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LABETALOL HYDROCHLORIDE
LABETALOL HYDROCHLORIDE - 16590-994-90 - (LABETALOL HYDROCHLORIDE)
Drug Information of LABETALOL HYDROCHLORIDE
| Product NDC: | 16590-994 |
| Proprietary Name: | LABETALOL HYDROCHLORIDE |
| Non Proprietary Name: | LABETALOL HYDROCHLORIDE |
| Active Ingredient(s): | 300 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: | 16590-994 |
| Labeler Name: | STAT RX USA LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA075133 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19980803 |
Package Information of LABETALOL HYDROCHLORIDE
| Package NDC: | 16590-994-90 |
| Package Description: | 90 TABLET, FILM COATED in 1 BOTTLE (16590-994-90) |
NDC Information of LABETALOL HYDROCHLORIDE
| NDC Code | 16590-994-90 |
| Proprietary Name | LABETALOL HYDROCHLORIDE |
| Package Description | 90 TABLET, FILM COATED in 1 BOTTLE (16590-994-90) |
| Product NDC | 16590-994 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | LABETALOL HYDROCHLORIDE |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 19980803 |
| Marketing Category Name | ANDA |
| Labeler Name | STAT RX USA LLC |
| Substance Name | LABETALOL HYDROCHLORIDE |
| Strength Number | 300 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC] |
