Package 66715-9819-7

Brand: ibuprofen

Generic: ibuprofen tablet, film-coated
NDC Package

Package Facts

Identity

Package NDC 66715-9819-7
Digits Only 6671598197
Product NDC 66715-9819
Description

50 POUCH in 1 BOX, UNIT-DOSE (66715-9819-7) / 2 TABLET, FILM COATED in 1 POUCH

Marketing

Marketing Status
Marketed Since 2014-09-12
Brand ibuprofen
Generic ibuprofen tablet, film-coated
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "e5bf5e09-7d43-6314-e053-2a95a90a2325", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "upc": ["0366715971975"], "unii": ["WK2XYI10QM"], "rxcui": ["310965"], "spl_set_id": ["e5bf5e09-7d42-6314-e053-2a95a90a2325"], "pharm_class_cs": ["Anti-Inflammatory Agents, Non-Steroidal [CS]"], "pharm_class_epc": ["Nonsteroidal Anti-inflammatory Drug [EPC]"], "pharm_class_moa": ["Cyclooxygenase Inhibitors [MoA]"], "manufacturer_name": ["Lil' Drug Store Products, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "50 POUCH in 1 BOX, UNIT-DOSE (66715-9819-7)  / 2 TABLET, FILM COATED in 1 POUCH", "package_ndc": "66715-9819-7", "marketing_start_date": "20140912"}], "brand_name": "Ibuprofen", "product_id": "66715-9819_e5bf5e09-7d43-6314-e053-2a95a90a2325", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "66715-9819", "generic_name": "Ibuprofen tablet, film-coated", "labeler_name": "Lil' Drug Store Products, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Ibuprofen", "active_ingredients": [{"name": "IBUPROFEN", "strength": "200 mg/1"}], "application_number": "ANDA075010", "marketing_category": "ANDA", "marketing_start_date": "20140912", "listing_expiration_date": "20261231"}