lactulose
Generic: lactulose
Labeler: pai holdings, llc dba pai pharmaDrug Facts
Product Profile
Brand Name
lactulose
Generic Name
lactulose
Labeler
pai holdings, llc dba pai pharma
Dosage Form
SOLUTION
Routes
Active Ingredients
lactulose 10 g/15mL
Manufacturer
Identifiers & Regulatory
Product NDC
0121-0873
Product ID
0121-0873_b73c2ddc-a690-46e1-aa89-40fa890c9ab4
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA074623
Listing Expiration
2026-12-31
Marketing Start
2019-12-03
Pharmacologic Class
Established (EPC)
Mechanism of Action
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
01210873
Hyphenated Format
0121-0873
Supplemental Identifiers
RxCUI
UNII
NUI
Packaging Origin
Original Packager
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
source: ndc
Resolved Composition
Strengths
- 10 g/15mL
Packaging
- 15 mL in 1 CUP, UNIT-DOSE (0121-0873-15)
- 473 mL in 1 BOTTLE (0121-0873-16)
- 946 mL in 1 BOTTLE (0121-0873-32)
Packages (3)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "b73c2ddc-a690-46e1-aa89-40fa890c9ab4", "openfda": {"nui": ["N0000175811", "N0000010288", "N0000175833", "N0000009871"], "unii": ["9U7D5QH5AE"], "rxcui": ["391937"], "spl_set_id": ["cbf0497c-9c8d-4dfa-bebd-64c589468401"], "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": ["PAI Holdings, LLC dba PAI Pharma"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "15 mL in 1 CUP, UNIT-DOSE (0121-0873-15)", "package_ndc": "0121-0873-15", "marketing_start_date": "20191203"}, {"sample": false, "description": "473 mL in 1 BOTTLE (0121-0873-16)", "package_ndc": "0121-0873-16", "marketing_start_date": "20191203"}, {"sample": false, "description": "946 mL in 1 BOTTLE (0121-0873-32)", "package_ndc": "0121-0873-32", "marketing_start_date": "20191203"}], "brand_name": "LACTULOSE", "product_id": "0121-0873_b73c2ddc-a690-46e1-aa89-40fa890c9ab4", "dosage_form": "SOLUTION", "pharm_class": ["Acidifying Activity [MoA]", "Osmotic Activity [MoA]", "Osmotic Laxative [EPC]", "Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]"], "product_ndc": "0121-0873", "generic_name": "Lactulose", "labeler_name": "PAI Holdings, LLC dba PAI Pharma", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "LACTULOSE", "active_ingredients": [{"name": "LACTULOSE", "strength": "10 g/15mL"}], "application_number": "ANDA074623", "marketing_category": "ANDA", "marketing_start_date": "20191203", "listing_expiration_date": "20261231"}