Labetalol (Sun Pharmaceutical Industries, Inc.)


Welcome to the PulseAid listing for the Labetalol drug offered from Sun Pharmaceutical Industries, Inc.. This Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC] pharmaceutical is classified as a HUMAN PRESCRIPTION DRUG. Below, you can view details for this drug, such as its dosage form, route of delivery, start market/end market dates, and more. We have also randomly listed additional pharmaceuticals used in the same HUMAN PRESCRIPTION DRUG drug type category.
LABELER NAME / MANUFACTURER: Sun Pharmaceutical Industries, Inc.
NON-PROPRIETARY NAME: Labetalol
SUBSTANCE NAME: LABETALOL
TYPE: HUMAN PRESCRIPTION DRUG
PHARMA CLASS: Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]
ROUTE: ORAL
DOSAGE FORM: TABLET, FILM COATED
MARKETING CATEGORY NAME: ANDA
START MARKETING DATE: 1999-07-29
END MARKETING DATE: 0000-00-00


Labetalol HUMAN PRESCRIPTION DRUG Details:

Item DescriptionLabetalol from Sun Pharmaceutical Industries, Inc.
LABELER NAME: Sun Pharmaceutical Industries, Inc.
DEA SCHEDULE:
ACTIVE STRENGTH: 100(mg/1)
START MARKETING DATE: 1999-07-29
END MARKETING DATE: 0000-00-00
PRODUCT ID: 57664-650_bea768de-b1a6-4fbe-8555-6d1ac6019f16
PRODUCT NDC: 57664-650
APPLICATION NUMBER: ANDA075215

Other LABETALOL Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Sun Pharmaceutical Industries, Inc.Labetalol