Package 64980-592-24

Brand: lactulose solution

Generic: lactulose solution usp, 10 g/15 ml
NDC Package

Package Facts

Identity

Package NDC 64980-592-24
Digits Only 6498059224
Product NDC 64980-592
Description

236 mL in 1 BOTTLE (64980-592-24)

Marketing

Marketing Status
Marketed Since 2023-05-25
Brand lactulose solution
Generic lactulose solution usp, 10 g/15 ml
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL", "RECTAL"], "spl_id": "ae4387e8-ba31-4378-9e67-98effdcc998f", "openfda": {"nui": ["N0000175811", "N0000010288", "N0000175833", "N0000009871"], "unii": ["9U7D5QH5AE"], "rxcui": ["391937"], "spl_set_id": ["e75c335b-f19e-42e2-a24f-d891a52d3d34"], "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": ["Rising Pharma Holdings, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "118 mL in 1 BOTTLE (64980-592-12)", "package_ndc": "64980-592-12", "marketing_start_date": "20230525"}, {"sample": false, "description": "236 mL in 1 BOTTLE (64980-592-24)", "package_ndc": "64980-592-24", "marketing_start_date": "20230525"}, {"sample": false, "description": "473 mL in 1 BOTTLE (64980-592-48)", "package_ndc": "64980-592-48", "marketing_start_date": "20230525"}, {"sample": false, "description": "946 mL in 1 BOTTLE (64980-592-95)", "package_ndc": "64980-592-95", "marketing_start_date": "20230525"}], "brand_name": "Lactulose Solution", "product_id": "64980-592_ae4387e8-ba31-4378-9e67-98effdcc998f", "dosage_form": "SOLUTION", "pharm_class": ["Acidifying Activity [MoA]", "Osmotic Activity [MoA]", "Osmotic Laxative [EPC]", "Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]"], "product_ndc": "64980-592", "generic_name": "Lactulose Solution USP, 10 g/15 mL", "labeler_name": "Rising Pharma Holdings, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lactulose Solution", "active_ingredients": [{"name": "LACTULOSE", "strength": "10 g/15mL"}], "application_number": "ANDA076645", "marketing_category": "ANDA", "marketing_start_date": "20211014", "listing_expiration_date": "20271231"}