Package 42708-175-30

Brand: ibuprofen

Generic: ibuprofen
NDC Package Sample

Package Facts

Identity

Package NDC 42708-175-30
Digits Only 4270817530
Product NDC 42708-175
Description

30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (42708-175-30)

Marketing

Marketing Status
Marketed Since 2023-06-20
Brand ibuprofen
Generic ibuprofen
Sample Package Yes

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "459bae98-33e9-56dd-e063-6394a90a48b8", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "unii": ["WK2XYI10QM"], "rxcui": ["197806"], "spl_set_id": ["fd8b82a7-96fe-8bf5-e053-6394a90a3935"], "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": ["QPharma Inc"]}, "finished": true, "packaging": [{"sample": true, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (42708-175-30)", "package_ndc": "42708-175-30", "marketing_start_date": "20230620"}], "brand_name": "Ibuprofen", "product_id": "42708-175_459bae98-33e9-56dd-e063-6394a90a48b8", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "42708-175", "generic_name": "Ibuprofen", "labeler_name": "QPharma Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ibuprofen", "active_ingredients": [{"name": "IBUPROFEN", "strength": "600 mg/1"}], "application_number": "ANDA091625", "marketing_category": "ANDA", "marketing_start_date": "20151221", "listing_expiration_date": "20261231"}