NDC 63629-8800

Enulose

Lactulose

Enulose is a Oral; Rectal Solution in the Human Prescription Drug category. It is labeled and distributed by Bryant Ranch Prepack. The primary component is Lactulose.

Product ID63629-8800_388176ba-c298-4737-9ced-bd197c131a1f
NDC63629-8800
Product TypeHuman Prescription Drug
Proprietary NameEnulose
Generic NameLactulose
Dosage FormSolution
Route of AdministrationORAL; RECTAL
Marketing Start Date2011-02-28
Marketing CategoryANDA /
Application NumberANDA090502
Labeler NameBryant Ranch Prepack
Substance NameLACTULOSE
Active Ingredient Strength10 g/15mL
Pharm ClassesAcidifying Activity [MoA], Osmotic Activity [MoA], Osmotic Laxative [EPC], Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]
NDC Exclude FlagN
Listing Certified Through2023-12-31

Packaging

NDC 63629-8800-1

473 mL in 1 BOTTLE (63629-8800-1)
Marketing Start Date2021-09-10
NDC Exclude FlagN
Sample Package?N

Drug Details

NDC Crossover Matching brand name "Enulose" or generic name "Lactulose"

NDCBrand NameGeneric Name
45963-438EnuloseEnulose
0116-4005LactuloseLactulose
0121-0577LACTULOSELACTULOSE
0121-0873LACTULOSELactulose
0121-1154LACTULOSELACTULOSE
0121-1746LACTULOSELACTULOSE
0121-4577LACTULOSELACTULOSE
0527-5120LACTULOSELACTULOSE
0527-5125LACTULOSELACTULOSE
0603-1378Lactuloselactulose
13668-574LactuloseLactulose
13668-580LactuloseLactulose

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