constulose

Generic: lactulose

Labeler: actavis pharma, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name constulose
Generic Name lactulose
Labeler actavis pharma, inc.
Dosage Form SOLUTION
Routes
ORAL
Active Ingredients

lactulose 10 g/15mL

Manufacturer
Actavis Pharma, Inc.

Identifiers & Regulatory

Product NDC 45963-439
Product ID 45963-439_7fd63ff0-fccd-408a-9c56-2c2fefdb74fc
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA090503
Listing Expiration 2026-12-31
Marketing Start 2011-02-28

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 45963439
Hyphenated Format 45963-439

Supplemental Identifiers

RxCUI
391937 544452
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 constulose (source: ndc)
Generic Name lactulose (source: ndc)
Application Number ANDA090503 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 g/15mL
source: ndc
Packaging
  • 237 mL in 1 BOTTLE (45963-439-63)
  • 946 mL in 1 BOTTLE (45963-439-65)
source: ndc

Packages (2)

Ingredients (1)

lactulose (10 g/15mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "7fd63ff0-fccd-408a-9c56-2c2fefdb74fc", "openfda": {"nui": ["N0000175811", "N0000010288", "N0000175833", "N0000009871"], "unii": ["9U7D5QH5AE"], "rxcui": ["391937", "544452"], "spl_set_id": ["461ec39f-eeb4-4460-9b5c-62367d47162b"], "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": ["Actavis Pharma, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "237 mL in 1 BOTTLE (45963-439-63)", "package_ndc": "45963-439-63", "marketing_start_date": "20110228"}, {"sample": false, "description": "946 mL in 1 BOTTLE (45963-439-65)", "package_ndc": "45963-439-65", "marketing_start_date": "20110228"}], "brand_name": "Constulose", "product_id": "45963-439_7fd63ff0-fccd-408a-9c56-2c2fefdb74fc", "dosage_form": "SOLUTION", "pharm_class": ["Acidifying Activity [MoA]", "Osmotic Activity [MoA]", "Osmotic Laxative [EPC]", "Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]"], "product_ndc": "45963-439", "generic_name": "Lactulose", "labeler_name": "Actavis Pharma, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Constulose", "active_ingredients": [{"name": "LACTULOSE", "strength": "10 g/15mL"}], "application_number": "ANDA090503", "marketing_category": "ANDA", "marketing_start_date": "20110228", "listing_expiration_date": "20261231"}