Package 62207-355-49

Brand: ibuprofen

Generic: ibuprofen
NDC Package

Package Facts

Identity

Package NDC 62207-355-49
Digits Only 6220735549
Product NDC 62207-355
Product ID 62207-355_44dee7dd-17ff-8faa-e063-6294a90a6712
Description

1000 TABLET, FILM COATED in 1 BOTTLE (62207-355-49)

Marketing

Marketing Status
Marketed Since 2015-09-21
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": "44dee7dd-17ff-8faa-e063-6294a90a6712", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "upc": ["0362207355544", "0362207356541", "0362207354547"], "unii": ["WK2XYI10QM"], "rxcui": ["197805", "197806", "197807"], "spl_set_id": ["8804564c-9e1b-43c1-8b58-fd6ace645f00"], "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": ["Granules India Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "50 TABLET, FILM COATED in 1 BOTTLE (62207-355-42)", "package_ndc": "62207-355-42", "marketing_start_date": "20150921"}, {"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (62207-355-43)", "package_ndc": "62207-355-43", "marketing_start_date": "20150921"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (62207-355-47)", "package_ndc": "62207-355-47", "marketing_start_date": "20150921"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (62207-355-49)", "package_ndc": "62207-355-49", "marketing_start_date": "20150921"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (62207-355-54)", "package_ndc": "62207-355-54", "marketing_start_date": "20150921"}], "brand_name": "Ibuprofen", "product_id": "62207-355_44dee7dd-17ff-8faa-e063-6294a90a6712", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "62207-355", "generic_name": "Ibuprofen", "labeler_name": "Granules India Limited", "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": "20150921", "listing_expiration_date": "20261231"}