lactulose

Generic: lactulose

Labeler: apozeal pharmaceuticals inc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name lactulose
Generic Name lactulose
Labeler apozeal pharmaceuticals inc
Dosage Form SOLUTION
Routes
ORAL RECTAL
Active Ingredients

lactulose 10 g/15mL

Manufacturer
APOZEAL PHARMACEUTICALS INC

Identifiers & Regulatory

Product NDC 83745-249
Product ID 83745-249_2341cf95-5e57-47ab-9dc3-73afa86b786d
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA203762
Listing Expiration 2027-12-31
Marketing Start 2024-12-20

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 83745249
Hyphenated Format 83745-249

Supplemental Identifiers

RxCUI
391937
UPC
0383745249324 0383745249089 0383745249164
UNII
9U7D5QH5AE
NUI
N0000175811 N0000010288 N0000175833 N0000009871

Packaging Origin

Original Packager
true

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 ANDA203762 (source: ndc)
Routes
ORAL RECTAL
source: ndc

Resolved Composition

Strengths
  • 10 g/15mL
source: ndc
Packaging
  • 237 mL in 1 BOTTLE (83745-249-08)
  • 473 mL in 1 BOTTLE (83745-249-16)
  • 946 mL in 1 BOTTLE (83745-249-32)
source: ndc

Packages (3)

83745-249-08 237 mL in 1 BOTTLE (83745-249-08) 83745-249-16 473 mL in 1 BOTTLE (83745-249-16) 83745-249-32 946 mL in 1 BOTTLE (83745-249-32)

Ingredients (1)

lactulose (10 g/15mL)

Linked Drug Pages (1)

Lactulose ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL", "RECTAL"], "spl_id": "2341cf95-5e57-47ab-9dc3-73afa86b786d", "openfda": {"nui": ["N0000175811", "N0000010288", "N0000175833", "N0000009871"], "upc": ["0383745249324", "0383745249089", "0383745249164"], "unii": ["9U7D5QH5AE"], "rxcui": ["391937"], "spl_set_id": ["a8af7389-3699-4873-b05a-509af7e8eaab"], "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": ["APOZEAL PHARMACEUTICALS INC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "237 mL in 1 BOTTLE (83745-249-08)", "package_ndc": "83745-249-08", "marketing_start_date": "20241220"}, {"sample": false, "description": "473 mL in 1 BOTTLE (83745-249-16)", "package_ndc": "83745-249-16", "marketing_start_date": "20241220"}, {"sample": false, "description": "946 mL in 1 BOTTLE (83745-249-32)", "package_ndc": "83745-249-32", "marketing_start_date": "20241220"}], "brand_name": "Lactulose", "product_id": "83745-249_2341cf95-5e57-47ab-9dc3-73afa86b786d", "dosage_form": "SOLUTION", "pharm_class": ["Acidifying Activity [MoA]", "Osmotic Activity [MoA]", "Osmotic Laxative [EPC]", "Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]"], "product_ndc": "83745-249", "generic_name": "Lactulose", "labeler_name": "APOZEAL PHARMACEUTICALS INC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lactulose", "active_ingredients": [{"name": "LACTULOSE", "strength": "10 g/15mL"}], "application_number": "ANDA203762", "marketing_category": "ANDA", "marketing_start_date": "20241220", "listing_expiration_date": "20271231"}