Lidocaine Hydrochloride and Dextrose (Hospira, Inc.)


Welcome to the PulseAid listing for the Lidocaine Hydrochloride and Dextrose drug offered from Hospira, Inc.. This Amide Local Anesthetic [EPC],Amides [Chemical/Ingredient],Antiarrhythmic [EPC],Local Anesthesia [PE] 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: Hospira, Inc.
NON-PROPRIETARY NAME: lidocaine hydrochloride and dextrose
SUBSTANCE NAME: LIDOCAINE HYDROCHLORIDE; DEXTROSE MONOHYDRATE
TYPE: HUMAN PRESCRIPTION DRUG
PHARMA CLASS: Amide Local Anesthetic [EPC],Amides [Chemical/Ingredient],Antiarrhythmic [EPC],Local Anesthesia [PE]
ROUTE: INTRASPINAL
DOSAGE FORM: INJECTION, SOLUTION
MARKETING CATEGORY NAME: ANDA
START MARKETING DATE: 2005-06-22
END MARKETING DATE: 0000-00-00


Lidocaine Hydrochloride and Dextrose HUMAN PRESCRIPTION DRUG Details:

Item DescriptionLidocaine Hydrochloride and Dextrose from Hospira, Inc.
LABELER NAME: Hospira, Inc.
DEA SCHEDULE:
ACTIVE STRENGTH: 50; 75(mg/mL; mg/mL)
START MARKETING DATE: 2005-06-22
END MARKETING DATE: 0000-00-00
PRODUCT ID: 0409-4712_a5e5b063-2407-426e-a5d0-1a3effa424dc
PRODUCT NDC: 0409-4712
APPLICATION NUMBER: ANDA083914

Other LIDOCAINE HYDROCHLORIDE; DEXTROSE MONOHYDRATE Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Hospira, Inc.Lidocaine Hydrochloride and Dextrose