Package 49483-612-01

Brand: ibuprofen

Generic: ibuprofen
NDC Package

Package Facts

Identity

Package NDC 49483-612-01
Digits Only 4948361201
Product NDC 49483-612
Description

100 TABLET, FILM COATED in 1 BOTTLE (49483-612-01)

Marketing

Marketing Status
Marketed Since 2016-11-16
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": "20b8a0bc-778a-7848-e063-6394a90ad512", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "upc": ["0349483612349"], "unii": ["WK2XYI10QM"], "rxcui": ["310965"], "spl_set_id": ["82aad715-f652-471b-840c-5151c66e5ade"], "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": ["TIME CAP LABORATORIES,INC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "6500 TABLET, FILM COATED in 1 BAG (49483-612-00)", "package_ndc": "49483-612-00", "marketing_start_date": "20161116"}, {"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (49483-612-01)", "package_ndc": "49483-612-01", "marketing_start_date": "20161116"}, {"sample": false, "description": "50 TABLET, FILM COATED in 1 BOTTLE (49483-612-05)", "package_ndc": "49483-612-05", "marketing_start_date": "20161116"}, {"sample": false, "description": "225 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (49483-612-34)", "package_ndc": "49483-612-34", "marketing_start_date": "20240830"}], "brand_name": "IBUPROFEN", "product_id": "49483-612_20b8a0bc-778a-7848-e063-6394a90ad512", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "49483-612", "generic_name": "IBUPROFEN", "labeler_name": "TIME CAP LABORATORIES,INC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "IBUPROFEN", "active_ingredients": [{"name": "IBUPROFEN", "strength": "200 mg/1"}], "application_number": "ANDA091237", "marketing_category": "ANDA", "marketing_start_date": "20161116", "listing_expiration_date": "20261231"}