kristalose

Generic: lactulose

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

Drug Facts

Product Profile

Brand Name kristalose
Generic Name lactulose
Labeler cumberland pharmaceuticals inc.
Dosage Form POWDER, FOR SOLUTION
Routes
ORAL
Active Ingredients

lactulose 20 g/20g

Manufacturer
Cumberland Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 66220-729
Product ID 66220-729_85528d56-e38f-4565-9136-c7639b479634
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA074712
Listing Expiration 2026-12-31
Marketing Start 2012-01-20

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 66220729
Hyphenated Format 66220-729

Supplemental Identifiers

RxCUI
1251190 1251192 1251194 1251196
UPC
0366220729016 0366220719017
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 kristalose (source: ndc)
Generic Name lactulose (source: ndc)
Application Number ANDA074712 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 g/20g
source: ndc
Packaging
  • 30 POUCH in 1 CARTON (66220-729-30) / 20 g in 1 POUCH (66220-729-01)
source: ndc

Packages (1)

66220-729-30 30 POUCH in 1 CARTON (66220-729-30) / 20 g in 1 POUCH (66220-729-01)

Ingredients (1)

lactulose (20 g/20g)

Linked Drug Pages (1)

KRISTALOSE ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "85528d56-e38f-4565-9136-c7639b479634", "openfda": {"nui": ["N0000175811", "N0000010288", "N0000175833", "N0000009871"], "upc": ["0366220729016", "0366220719017"], "unii": ["9U7D5QH5AE"], "rxcui": ["1251190", "1251192", "1251194", "1251196"], "spl_set_id": ["535dd1ea-b567-49f7-9a84-8ea91e78c466"], "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": ["Cumberland Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 POUCH in 1 CARTON (66220-729-30)  / 20 g in 1 POUCH (66220-729-01)", "package_ndc": "66220-729-30", "marketing_start_date": "20120120"}], "brand_name": "KRISTALOSE", "product_id": "66220-729_85528d56-e38f-4565-9136-c7639b479634", "dosage_form": "POWDER, FOR SOLUTION", "pharm_class": ["Acidifying Activity [MoA]", "Osmotic Activity [MoA]", "Osmotic Laxative [EPC]", "Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]"], "product_ndc": "66220-729", "generic_name": "lactulose", "labeler_name": "Cumberland Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "KRISTALOSE", "active_ingredients": [{"name": "LACTULOSE", "strength": "20 g/20g"}], "application_number": "ANDA074712", "marketing_category": "ANDA", "marketing_start_date": "20120120", "listing_expiration_date": "20261231"}