Package 55111-683-01

Brand: ibu

Generic: ibuprofen
NDC Package

Package Facts

Identity

Package NDC 55111-683-01
Digits Only 5511168301
Product NDC 55111-683
Description

100 TABLET in 1 BOTTLE (55111-683-01)

Marketing

Marketing Status
Marketed Since 2008-11-20
Brand ibu
Generic ibuprofen
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "a7977972-4353-9ca0-d419-e37039010e7d", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "unii": ["WK2XYI10QM"], "rxcui": ["197805", "197806", "197807", "206905", "206913", "206917"], "spl_set_id": ["24731405-219c-79b4-ecf0-7d5fbfda94ba"], "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": ["Dr. Reddy's Laboratories Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (55111-683-01)", "package_ndc": "55111-683-01", "marketing_start_date": "20081120"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (55111-683-05)", "package_ndc": "55111-683-05", "marketing_start_date": "20081120"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (55111-683-09)", "package_ndc": "55111-683-09", "marketing_start_date": "20081120"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (55111-683-30)", "package_ndc": "55111-683-30", "marketing_start_date": "20081120"}, {"sample": false, "description": "50 TABLET in 1 BOTTLE (55111-683-50)", "package_ndc": "55111-683-50", "marketing_start_date": "20081120"}], "brand_name": "IBU", "product_id": "55111-683_a7977972-4353-9ca0-d419-e37039010e7d", "dosage_form": "TABLET", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "55111-683", "generic_name": "Ibuprofen", "labeler_name": "Dr. Reddy's Laboratories Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "IBU", "active_ingredients": [{"name": "IBUPROFEN", "strength": "600 mg/1"}], "application_number": "ANDA075682", "marketing_category": "ANDA", "marketing_start_date": "20081120", "listing_expiration_date": "20261231"}