lactulose

Generic: lactulose

Labeler: lannett company, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name lactulose
Generic Name lactulose
Labeler lannett company, inc.
Dosage Form SOLUTION
Routes
ORAL
Active Ingredients

lactulose 10 g/15mL

Manufacturer
Lannett Company, Inc.

Identifiers & Regulatory

Product NDC 0527-5125
Product ID 0527-5125_1b869904-b3c5-4f81-a333-1f26b6b2c7bf
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA075993
Listing Expiration 2026-12-31
Marketing Start 2001-07-26

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 05275125
Hyphenated Format 0527-5125

Supplemental Identifiers

RxCUI
391937
UPC
0305275125701
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 ANDA075993 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 g/15mL
source: ndc
Packaging
  • 237 mL in 1 BOTTLE (0527-5125-68)
  • 473 mL in 1 BOTTLE (0527-5125-70)
  • 946 mL in 1 BOTTLE (0527-5125-78)
  • 1892 mL in 1 BOTTLE (0527-5125-82)
source: ndc

Packages (4)

0527-5125-68 237 mL in 1 BOTTLE (0527-5125-68) 0527-5125-70 473 mL in 1 BOTTLE (0527-5125-70) 0527-5125-78 946 mL in 1 BOTTLE (0527-5125-78) 0527-5125-82 1892 mL in 1 BOTTLE (0527-5125-82)

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"], "spl_id": "1b869904-b3c5-4f81-a333-1f26b6b2c7bf", "openfda": {"nui": ["N0000175811", "N0000010288", "N0000175833", "N0000009871"], "upc": ["0305275125701"], "unii": ["9U7D5QH5AE"], "rxcui": ["391937"], "spl_set_id": ["6619b25c-26b7-4c43-8c4f-9d33a23c61ca"], "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": ["Lannett Company, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "237 mL in 1 BOTTLE (0527-5125-68)", "package_ndc": "0527-5125-68", "marketing_start_date": "20010726"}, {"sample": false, "description": "473 mL in 1 BOTTLE (0527-5125-70)", "package_ndc": "0527-5125-70", "marketing_start_date": "20010726"}, {"sample": false, "description": "946 mL in 1 BOTTLE (0527-5125-78)", "package_ndc": "0527-5125-78", "marketing_start_date": "20010726"}, {"sample": false, "description": "1892 mL in 1 BOTTLE (0527-5125-82)", "package_ndc": "0527-5125-82", "marketing_start_date": "20010726"}], "brand_name": "LACTULOSE", "product_id": "0527-5125_1b869904-b3c5-4f81-a333-1f26b6b2c7bf", "dosage_form": "SOLUTION", "pharm_class": ["Acidifying Activity [MoA]", "Osmotic Activity [MoA]", "Osmotic Laxative [EPC]", "Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]"], "product_ndc": "0527-5125", "generic_name": "LACTULOSE", "labeler_name": "Lannett Company, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "LACTULOSE", "active_ingredients": [{"name": "LACTULOSE", "strength": "10 g/15mL"}], "application_number": "ANDA075993", "marketing_category": "ANDA", "marketing_start_date": "20010726", "listing_expiration_date": "20261231"}