Package 0761-0908-04

Brand: ibuprofen 200 mg

Generic: ibuprofen
NDC Package

Package Facts

Identity

Package NDC 0761-0908-04
Digits Only 0761090804
Product NDC 0761-0908
Description

250 TABLET in 1 BOTTLE (0761-0908-04)

Marketing

Marketing Status
Marketed Since 2021-12-15
Brand ibuprofen 200 mg
Generic ibuprofen
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "0e12b3c6-3579-b0dc-e063-6394a90a8ea4", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "unii": ["WK2XYI10QM"], "rxcui": ["310965"], "spl_set_id": ["d3351d44-2078-3adc-e053-2995a90a3c8f"], "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": ["Basic Drugs, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "250 TABLET in 1 BOTTLE (0761-0908-04)", "package_ndc": "0761-0908-04", "marketing_start_date": "20211215"}], "brand_name": "IBUPROFEN 200 MG", "product_id": "0761-0908_0e12b3c6-3579-b0dc-e063-6394a90a8ea4", "dosage_form": "TABLET", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "0761-0908", "generic_name": "IBUPROFEN", "labeler_name": "Basic Drugs, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "IBUPROFEN", "brand_name_suffix": "200 MG", "active_ingredients": [{"name": "IBUPROFEN", "strength": "200 mg/1"}], "application_number": "ANDA079174", "marketing_category": "ANDA", "marketing_start_date": "20211214", "listing_expiration_date": "20261231"}