Package 68071-4949-3

Brand: ibuprofen

Generic: ibuprofen
NDC Package

Package Facts

Identity

Package NDC 68071-4949-3
Digits Only 6807149493
Product NDC 68071-4949
Description

3 TABLET, FILM COATED in 1 BOTTLE (68071-4949-3)

Marketing

Marketing Status
Marketed Since 2019-06-26
Brand ibuprofen
Generic ibuprofen
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "1b2e2e40-6137-401a-e063-6294a90a8c8f", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "upc": ["0368071494938"], "unii": ["WK2XYI10QM"], "rxcui": ["197807"], "spl_set_id": ["8c3dccbb-1084-cd09-e053-2a95a90ac12a"], "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": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "3 TABLET, FILM COATED in 1 BOTTLE (68071-4949-3)", "package_ndc": "68071-4949-3", "marketing_start_date": "20190626"}], "brand_name": "Ibuprofen", "product_id": "68071-4949_1b2e2e40-6137-401a-e063-6294a90a8c8f", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "68071-4949", "generic_name": "Ibuprofen", "labeler_name": "NuCare Pharmaceuticals,Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ibuprofen", "active_ingredients": [{"name": "IBUPROFEN", "strength": "800 mg/1"}], "application_number": "ANDA078329", "marketing_category": "ANDA", "marketing_start_date": "20140401", "listing_expiration_date": "20261231"}