Package 21130-393-14

Brand: ibuprofen

Generic: ibuprofen
NDC Package

Package Facts

Identity

Package NDC 21130-393-14
Digits Only 2113039314
Product NDC 21130-393
Description

500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (21130-393-14)

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": "1cf05f98-9303-4cd8-8f0f-1b45767b0613", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "upc": ["0321130787754"], "unii": ["WK2XYI10QM"], "rxcui": ["310965"], "spl_set_id": ["45520969-7a2d-4469-ba25-7db160d50ccf"], "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": ["Better Living Brands, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (21130-393-14)", "package_ndc": "21130-393-14", "marketing_start_date": "19990301"}], "brand_name": "Ibuprofen", "product_id": "21130-393_1cf05f98-9303-4cd8-8f0f-1b45767b0613", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "21130-393", "generic_name": "Ibuprofen", "labeler_name": "Better Living Brands, LLC", "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"}