Package 0121-1746-00
Brand: lactulose
Generic: lactulosePackage Facts
Identity
Package NDC
0121-1746-00
Digits Only
0121174600
Product NDC
0121-1746
Description
10 TRAY in 1 CASE (0121-1746-00) / 10 CUP, UNIT-DOSE in 1 TRAY / 30 mL in 1 CUP, UNIT-DOSE (0121-1746-30)
Marketing
Marketing Status
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": "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": "10 TRAY in 1 CASE (0121-1746-00) / 10 CUP, UNIT-DOSE in 1 TRAY / 30 mL in 1 CUP, UNIT-DOSE (0121-1746-30)", "package_ndc": "0121-1746-00", "marketing_start_date": "20191203"}, {"sample": false, "description": "6 CARTON in 1 CASE (0121-1746-06) / 16 CUP, UNIT-DOSE in 1 CARTON / 30 mL in 1 CUP, UNIT-DOSE (0121-1746-30)", "package_ndc": "0121-1746-06", "marketing_start_date": "20191203"}, {"sample": false, "description": "4 TRAY in 1 CASE (0121-1746-40) / 10 CUP, UNIT-DOSE in 1 TRAY / 30 mL in 1 CUP, UNIT-DOSE (0121-1746-30)", "package_ndc": "0121-1746-40", "marketing_start_date": "20191203"}], "brand_name": "LACTULOSE", "product_id": "0121-1746_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": "0121-1746", "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/30mL"}], "application_number": "ANDA074623", "marketing_category": "ANDA", "marketing_start_date": "20191203", "listing_expiration_date": "20261231"}