lactulose

Generic: lactulose

Labeler: cardinal health 107, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name lactulose
Generic Name lactulose
Labeler cardinal health 107, llc
Dosage Form SOLUTION
Routes
ORAL
Active Ingredients

lactulose 20 g/30mL

Manufacturer
Cardinal Health 107, LLC

Identifiers & Regulatory

Product NDC 55154-9448
Product ID 55154-9448_c6c822e7-9486-4ad9-81a2-c2b8ee692f32
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA074623
Listing Expiration 2027-12-31
Marketing Start 1966-07-30

Pharmacologic Class

Established (EPC)
osmotic laxative [epc]
Mechanism of Action
osmotic activity [moa] acidifying activity [moa]
Physiologic Effect
stimulation large intestine fluid/electrolyte secretion [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 551549448
Hyphenated Format 55154-9448

Supplemental Identifiers

RxCUI
391937
UPC
0055154944854
UNII
9U7D5QH5AE
NUI
N0000175811 N0000010288 N0000175833 N0000009871

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name lactulose (source: ndc)
Generic Name lactulose (source: ndc)
Application Number ANDA074623 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 g/30mL
source: ndc
Packaging
  • 5 CUP, UNIT-DOSE in 1 BAG (55154-9448-5) / 30 mL in 1 CUP, UNIT-DOSE
source: ndc

Packages (1)

Ingredients (1)

lactulose (20 g/30mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "c6c822e7-9486-4ad9-81a2-c2b8ee692f32", "openfda": {"nui": ["N0000175811", "N0000010288", "N0000175833", "N0000009871"], "upc": ["0055154944854"], "unii": ["9U7D5QH5AE"], "rxcui": ["391937"], "spl_set_id": ["3cf3ff7c-67e7-42a9-8ebb-bd6c53937dd7"], "pharm_class_pe": ["Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]"], "pharm_class_epc": ["Osmotic Laxative [EPC]"], "pharm_class_moa": ["Osmotic Activity [MoA]", "Acidifying Activity [MoA]"], "manufacturer_name": ["Cardinal Health 107, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "5 CUP, UNIT-DOSE in 1 BAG (55154-9448-5)  / 30 mL in 1 CUP, UNIT-DOSE", "package_ndc": "55154-9448-5", "marketing_start_date": "19660730"}], "brand_name": "LACTULOSE", "product_id": "55154-9448_c6c822e7-9486-4ad9-81a2-c2b8ee692f32", "dosage_form": "SOLUTION", "pharm_class": ["Acidifying Activity [MoA]", "Osmotic Activity [MoA]", "Osmotic Laxative [EPC]", "Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]"], "product_ndc": "55154-9448", "generic_name": "LACTULOSE", "labeler_name": "Cardinal Health 107, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "LACTULOSE", "active_ingredients": [{"name": "LACTULOSE", "strength": "20 g/30mL"}], "application_number": "ANDA074623", "marketing_category": "ANDA", "marketing_start_date": "19660730", "listing_expiration_date": "20271231"}