Package 76282-713-55

Brand: ibuprofen

Generic: ibuprofen
NDC Package

Package Facts

Identity

Package NDC 76282-713-55
Digits Only 7628271355
Product NDC 76282-713
Product ID 76282-713_bc309c22-f359-42b1-86db-3970a5d53bc4
Description

1000 TABLET, FILM COATED in 1 BOTTLE (76282-713-55)

Marketing

Marketing Status
Marketed Since 2022-03-10
Brand ibuprofen
Generic ibuprofen
Sample Package No

Linked Drug Pages (1)

Ibuprofen ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "bc309c22-f359-42b1-86db-3970a5d53bc4", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "upc": ["0376282714554", "0376282712109", "0376282714905", "0376282713502", "0376282714103", "0376282714301", "0376282713106", "0376282713557", "0376282714509", "0376282712550", "0376282712505"], "unii": ["WK2XYI10QM"], "rxcui": ["197805", "197806", "197807"], "spl_set_id": ["362f934a-4382-43bc-bedd-65081286f1c9"], "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": ["EXELAN PHARMACEUTICALS, INC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (76282-713-10)", "package_ndc": "76282-713-10", "marketing_start_date": "20220310"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (76282-713-50)", "package_ndc": "76282-713-50", "marketing_start_date": "20220310"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (76282-713-55)", "package_ndc": "76282-713-55", "marketing_start_date": "20220310"}], "brand_name": "Ibuprofen", "product_id": "76282-713_bc309c22-f359-42b1-86db-3970a5d53bc4", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "76282-713", "generic_name": "Ibuprofen", "labeler_name": "EXELAN PHARMACEUTICALS, INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ibuprofen", "active_ingredients": [{"name": "IBUPROFEN", "strength": "600 mg/1"}], "application_number": "ANDA091625", "marketing_category": "ANDA", "marketing_start_date": "20220310", "listing_expiration_date": "20261231"}