Package 51672-2130-8

Brand: ibuprofen

Generic: ibuprofen
NDC Package

Package Facts

Identity

Package NDC 51672-2130-8
Digits Only 5167221308
Product NDC 51672-2130
Description

1 BOTTLE in 1 CARTON (51672-2130-8) / 120 mL in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2017-06-27
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": "39623a94-8b73-17c6-e063-6294a90a4c31", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "unii": ["WK2XYI10QM"], "rxcui": ["197803"], "spl_set_id": ["f4dad3d6-1366-4bdf-99eb-370ab74a6b9e"], "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": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (51672-2130-1)  / 240 mL in 1 BOTTLE", "package_ndc": "51672-2130-1", "marketing_start_date": "20170627"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (51672-2130-8)  / 120 mL in 1 BOTTLE", "package_ndc": "51672-2130-8", "marketing_start_date": "20170627"}], "brand_name": "Ibuprofen", "product_id": "51672-2130_39623a94-8b73-17c6-e063-6294a90a4c31", "dosage_form": "SUSPENSION", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "51672-2130", "generic_name": "Ibuprofen", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Ibuprofen", "active_ingredients": [{"name": "IBUPROFEN", "strength": "100 mg/5mL"}], "application_number": "ANDA209207", "marketing_category": "ANDA", "marketing_start_date": "20170627", "listing_expiration_date": "20261231"}