Package 0121-1930-30

Brand: lactulose

Generic: lactulose
NDC Package

Package Facts

Identity

Package NDC 0121-1930-30
Digits Only 0121193030
Product NDC 0121-1930
Description

30 POUCH in 1 CARTON (0121-1930-30) / 20 g in 1 POUCH (0121-1930-01)

Marketing

Marketing Status
Marketed Since 2025-03-17
Brand lactulose
Generic lactulose
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "e4873a34-cdc0-4c96-b04f-c84641f52236", "openfda": {"nui": ["N0000175811", "N0000010288", "N0000175833", "N0000009871"], "unii": ["9U7D5QH5AE"], "rxcui": ["1251190", "1251194"], "spl_set_id": ["5ae4b6da-44df-419a-9f2b-8c4d79f635c8"], "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": "30 POUCH in 1 CARTON (0121-1930-30)  / 20 g in 1 POUCH (0121-1930-01)", "package_ndc": "0121-1930-30", "marketing_start_date": "20250317"}], "brand_name": "Lactulose", "product_id": "0121-1930_e4873a34-cdc0-4c96-b04f-c84641f52236", "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": "0121-1930", "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": "20 g/20g"}], "application_number": "ANDA217914", "marketing_category": "ANDA", "marketing_start_date": "20250317", "listing_expiration_date": "20261231"}