Package 62135-002-78
Brand: lactulose
Generic: lactulosePackage Facts
Identity
Package NDC
62135-002-78
Digits Only
6213500278
Product NDC
62135-002
Description
3785 mL in 1 PACKAGE (62135-002-78)
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": "49798265-6d70-8bc1-e063-6394a90a59d4", "openfda": {"nui": ["N0000175811", "N0000010288", "N0000175833", "N0000009871"], "upc": ["0362135002947", "0362135002374", "0362135002473", "0362135002787"], "unii": ["9U7D5QH5AE"], "rxcui": ["391937"], "spl_set_id": ["d6975cd8-80e0-43e2-809a-175ea7e40715"], "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": ["Chartwell RX, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2 TRAY in 1 BOX (62135-002-24) / 10 CUP, UNIT-DOSE in 1 TRAY / 15 mL in 1 CUP, UNIT-DOSE (62135-002-51)", "package_ndc": "62135-002-24", "marketing_start_date": "20240319"}, {"sample": false, "description": "237 mL in 1 PACKAGE (62135-002-37)", "package_ndc": "62135-002-37", "marketing_start_date": "20240319"}, {"sample": false, "description": "473 mL in 1 PACKAGE (62135-002-47)", "package_ndc": "62135-002-47", "marketing_start_date": "20240319"}, {"sample": false, "description": "3785 mL in 1 PACKAGE (62135-002-78)", "package_ndc": "62135-002-78", "marketing_start_date": "20240319"}, {"sample": false, "description": "946 mL in 1 PACKAGE (62135-002-94)", "package_ndc": "62135-002-94", "marketing_start_date": "20240319"}], "brand_name": "Lactulose", "product_id": "62135-002_49798265-6d70-8bc1-e063-6394a90a59d4", "dosage_form": "SOLUTION", "pharm_class": ["Acidifying Activity [MoA]", "Osmotic Activity [MoA]", "Osmotic Laxative [EPC]", "Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]"], "product_ndc": "62135-002", "generic_name": "Lactulose", "labeler_name": "Chartwell RX, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lactulose", "active_ingredients": [{"name": "LACTULOSE", "strength": "10 g/15mL"}], "application_number": "ANDA209517", "marketing_category": "ANDA", "marketing_start_date": "20181123", "listing_expiration_date": "20271231"}