Lomotil (RedPharm Drug, Inc.)


Welcome to the PulseAid listing for the Lomotil drug offered from RedPharm Drug, Inc.. This Anticholinergic [EPC],Cholinergic Antagonists [MoA],Cholinergic Muscarinic Antagonist [EPC],Cholinergic Muscarinic Antagonists [MoA],Antidiarrheal [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: RedPharm Drug, Inc.
NON-PROPRIETARY NAME: Lomotil
SUBSTANCE NAME: ATROPINE SULFATE; DIPHENOXYLATE HYDROCHLORIDE
TYPE: HUMAN PRESCRIPTION DRUG
PHARMA CLASS: Anticholinergic [EPC],Cholinergic Antagonists [MoA],Cholinergic Muscarinic Antagonist [EPC],Cholinergic Muscarinic Antagonists [MoA],Antidiarrheal [EPC]
ROUTE: ORAL
DOSAGE FORM: TABLET
MARKETING CATEGORY NAME: NDA
START MARKETING DATE: 1960-09-15
END MARKETING DATE: 0000-00-00


Lomotil HUMAN PRESCRIPTION DRUG Details:

Item DescriptionLomotil from RedPharm Drug, Inc.
LABELER NAME: RedPharm Drug, Inc.
DEA SCHEDULE: CV
ACTIVE STRENGTH: .025; 2.5(mg/1; mg/1)
START MARKETING DATE: 1960-09-15
END MARKETING DATE: 0000-00-00
PRODUCT ID: 67296-1210_4f1bbc1d-9586-20b2-e054-00144ff88e88
PRODUCT NDC: 67296-1210
APPLICATION NUMBER: NDA012462

Other ATROPINE SULFATE; DIPHENOXYLATE HYDROCHLORIDE Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
RedPharm Drug, Inc.Lomotil