Package 53746-137-30

Brand: ibuprofen

Generic: ibuprofen
NDC Package

Package Facts

Identity

Package NDC 53746-137-30
Digits Only 5374613730
Product NDC 53746-137
Description

30 TABLET in 1 BOTTLE (53746-137-30)

Marketing

Marketing Status
Marketed Since 2009-01-05
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": "32dbe366-3f8b-4ace-9ce4-a9b695c58d30", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "upc": ["0353746137012"], "unii": ["WK2XYI10QM"], "rxcui": ["197807"], "spl_set_id": ["75d963b9-3675-44ff-bc6b-83461bed1b67"], "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": ["Amneal Pharmaceuticals of New York LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (53746-137-01)", "package_ndc": "53746-137-01", "marketing_start_date": "20090105"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (53746-137-05)", "package_ndc": "53746-137-05", "marketing_start_date": "20090105"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (53746-137-30)", "package_ndc": "53746-137-30", "marketing_start_date": "20090105"}, {"sample": false, "description": "50 TABLET in 1 BOTTLE (53746-137-50)", "package_ndc": "53746-137-50", "marketing_start_date": "20090105"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (53746-137-60)", "package_ndc": "53746-137-60", "marketing_start_date": "20090105"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (53746-137-90)", "package_ndc": "53746-137-90", "marketing_start_date": "20090105"}], "brand_name": "Ibuprofen", "product_id": "53746-137_32dbe366-3f8b-4ace-9ce4-a9b695c58d30", "dosage_form": "TABLET", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "53746-137", "generic_name": "Ibuprofen", "labeler_name": "Amneal Pharmaceuticals of New York LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ibuprofen", "active_ingredients": [{"name": "IBUPROFEN", "strength": "800 mg/1"}], "application_number": "ANDA071935", "marketing_category": "ANDA", "marketing_start_date": "20090105", "listing_expiration_date": "20261231"}