Package 41250-993-20

Brand: ibuprofen

Generic: ibuprofen
NDC Package

Package Facts

Identity

Package NDC 41250-993-20
Digits Only 4125099320
Product NDC 41250-993
Description

225 TABLET, FILM COATED in 1 BOTTLE (41250-993-20)

Marketing

Marketing Status
Marketed Since 1999-03-01
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": "8a8f087d-f8bb-4e62-99d3-dfe28a6a7a0f", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "upc": ["0713733981132"], "unii": ["WK2XYI10QM"], "rxcui": ["310965"], "spl_set_id": ["36f7227d-f3cb-44b7-a4c1-27611cd15052"], "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": ["Meijer Distribution Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "225 TABLET, FILM COATED in 1 BOTTLE (41250-993-20)", "package_ndc": "41250-993-20", "marketing_start_date": "19990301"}, {"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (41250-993-91)", "package_ndc": "41250-993-91", "marketing_start_date": "19990301"}], "brand_name": "Ibuprofen", "product_id": "41250-993_8a8f087d-f8bb-4e62-99d3-dfe28a6a7a0f", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "41250-993", "generic_name": "Ibuprofen", "labeler_name": "Meijer Distribution Inc", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Ibuprofen", "active_ingredients": [{"name": "IBUPROFEN", "strength": "200 mg/1"}], "application_number": "ANDA075139", "marketing_category": "ANDA", "marketing_start_date": "19990301", "listing_expiration_date": "20261231"}