Lactulose
Lactulose Solution, USP
Approved
Approval ID
6c8f865e-f2f4-4c98-8bad-68f1575e2ed5
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Nov 4, 2019
Manufacturers
FDA
Morton Grove Pharmaceuticals, Inc.
DUNS: 801897505
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
Lactulose
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code60432-037
Application NumberANDA074602
Product Classification
M
Marketing Category
C73584
G
Generic Name
Lactulose
Product Specifications
Route of AdministrationORAL
Effective DateNovember 4, 2019
FDA Product Classification
INGREDIENTS (1)
LACTULOSEActive
Quantity: 10 g in 15 mL
Code: 9U7D5QH5AE
Classification: ACTIB