Package 66220-719-30

Brand: kristalose

Generic: lactulose
NDC Package

Package Facts

Identity

Package NDC 66220-719-30
Digits Only 6622071930
Product NDC 66220-719
Description

30 POUCH in 1 CARTON (66220-719-30) / 10 g in 1 POUCH (66220-719-01)

Marketing

Marketing Status
Marketed Since 2012-01-20
Brand kristalose
Generic lactulose
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "85528d56-e38f-4565-9136-c7639b479634", "openfda": {"nui": ["N0000175811", "N0000010288", "N0000175833", "N0000009871"], "upc": ["0366220729016", "0366220719017"], "unii": ["9U7D5QH5AE"], "rxcui": ["1251190", "1251192", "1251194", "1251196"], "spl_set_id": ["535dd1ea-b567-49f7-9a84-8ea91e78c466"], "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": ["Cumberland Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 POUCH in 1 CARTON (66220-719-30)  / 10 g in 1 POUCH (66220-719-01)", "package_ndc": "66220-719-30", "marketing_start_date": "20120120"}], "brand_name": "KRISTALOSE", "product_id": "66220-719_85528d56-e38f-4565-9136-c7639b479634", "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": "66220-719", "generic_name": "lactulose", "labeler_name": "Cumberland Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "KRISTALOSE", "active_ingredients": [{"name": "LACTULOSE", "strength": "10 g/10g"}], "application_number": "ANDA074712", "marketing_category": "ANDA", "marketing_start_date": "20120120", "listing_expiration_date": "20261231"}