lactulose

Generic: lactulose

Labeler: foxland pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name lactulose
Generic Name lactulose
Labeler foxland pharmaceuticals, inc.
Dosage Form SOLUTION
Routes
ORAL
Active Ingredients

lactulose 10 g/10g

Manufacturer
Foxland Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 69067-010
Product ID 69067-010_4618824a-2b40-3d54-e063-6394a90a4b96
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA074712
Listing Expiration 2026-12-31
Marketing Start 2018-09-21

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 69067010
Hyphenated Format 69067-010

Supplemental Identifiers

RxCUI
1251190 1251194
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 ANDA074712 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 g/10g
source: ndc
Packaging
  • 15 POUCH in 1 CARTON (69067-010-15) / 10 g in 1 POUCH
source: ndc

Packages (1)

69067-010-15 15 POUCH in 1 CARTON (69067-010-15) / 10 g in 1 POUCH

Ingredients (1)

lactulose (10 g/10g)

Linked Drug Pages (1)

Lactulose ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "4618824a-2b40-3d54-e063-6394a90a4b96", "openfda": {"nui": ["N0000175811", "N0000010288", "N0000175833", "N0000009871"], "unii": ["9U7D5QH5AE"], "rxcui": ["1251190", "1251194"], "spl_set_id": ["3363bdbd-f0d1-45b3-8193-7fdb0a310cc2"], "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": ["Foxland Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "15 POUCH in 1 CARTON (69067-010-15)  / 10 g in 1 POUCH", "package_ndc": "69067-010-15", "marketing_start_date": "20180921"}], "brand_name": "Lactulose", "product_id": "69067-010_4618824a-2b40-3d54-e063-6394a90a4b96", "dosage_form": "SOLUTION", "pharm_class": ["Acidifying Activity [MoA]", "Osmotic Activity [MoA]", "Osmotic Laxative [EPC]", "Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]"], "product_ndc": "69067-010", "generic_name": "Lactulose", "labeler_name": "Foxland Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lactulose", "active_ingredients": [{"name": "LACTULOSE", "strength": "10 g/10g"}], "application_number": "ANDA074712", "marketing_category": "ANDA", "marketing_start_date": "20180921", "listing_expiration_date": "20261231"}