MedPath

ANTICHOLIUM

ANTICHOLIUM solution for injection or infusion

Approved
Approval ID

b90b50e8-c8f1-4f2d-be6e-4d269b8c362c

Product Type

HUMAN PRESCRIPTION DRUG LABEL

Effective Date

Sep 14, 2023

Manufacturers
FDA

Provepharm Inc.

DUNS: 086861066

Products 1

Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.

physostigmine salicylate

Product Details

FDA regulatory identification and product classification information

FDA Identifiers
NDC Product Code81284-831
Product Classification
G
Generic Name
physostigmine salicylate
Product Specifications
Route of AdministrationINTRAVENOUS
Effective DateSeptember 14, 2023
FDA Product Classification

INGREDIENTS (5)

EDETATE SODIUMInactive
Code: MP1J8420LU
Classification: IACT
SODIUM HYDROXIDEInactive
Code: 55X04QC32I
Classification: IACT
WATERInactive
Code: 059QF0KO0R
Classification: IACT
HYDROCHLORIC ACIDInactive
Code: QTT17582CB
Classification: IACT
PHYSOSTIGMINE SALICYLATEActive
Quantity: 0.4 mg in 1 mL
Code: 2046ZRO9VU
Classification: ACTIB

MedPath

Empowering clinical research with data-driven insights and AI-powered tools.

© 2025 MedPath, Inc. All rights reserved.

ANTICHOLIUM - FDA Drug Approval Details