Package 18124-002-16

Brand: lactulose

Generic: lactulose
NDC Package

Package Facts

Identity

Package NDC 18124-002-16
Digits Only 1812400216
Product NDC 18124-002
Product ID 18124-002_d95ab755-1c2e-4124-8ed7-075936257c25
Description

473 mL in 1 BOTTLE (18124-002-16)

Marketing

Marketing Status
Marketed Since 2012-12-10
Brand lactulose
Generic lactulose
Sample Package No

Linked Drug Pages (1)

Lactulose ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL", "RECTAL"], "spl_id": "d95ab755-1c2e-4124-8ed7-075936257c25", "openfda": {"nui": ["N0000175811", "N0000010288", "N0000175833", "N0000009871"], "unii": ["9U7D5QH5AE"], "rxcui": ["391937"], "spl_set_id": ["a89835c9-8ce5-4627-8d7d-70ff175b2e07"], "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": ["Fresenius Kabi Austria GmbH"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "473 mL in 1 BOTTLE (18124-002-16)", "package_ndc": "18124-002-16", "marketing_start_date": "20121210"}], "brand_name": "Lactulose", "product_id": "18124-002_d95ab755-1c2e-4124-8ed7-075936257c25", "dosage_form": "SOLUTION", "pharm_class": ["Acidifying Activity [MoA]", "Osmotic Activity [MoA]", "Osmotic Laxative [EPC]", "Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]"], "product_ndc": "18124-002", "generic_name": "Lactulose", "labeler_name": "Fresenius Kabi Austria GmbH", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lactulose", "active_ingredients": [{"name": "LACTULOSE", "strength": "10 g/15mL"}], "application_number": "ANDA090502", "marketing_category": "ANDA", "marketing_start_date": "20121210", "listing_expiration_date": "20261231"}