Package 36800-193-83

Brand: ibuprofen

Generic: ibuprofen
NDC Package

Package Facts

Identity

Package NDC 36800-193-83
Digits Only 3680019383
Product NDC 36800-193
Description

300 CAPSULE, LIQUID FILLED in 1 BOTTLE (36800-193-83)

Marketing

Marketing Status
Marketed Since 2025-10-31
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": "427b861c-4464-a4b3-e063-6394a90aefb5", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "unii": ["WK2XYI10QM"], "rxcui": ["310964"], "spl_set_id": ["c6297c23-3b27-c0c6-e053-2995a90a3e76"], "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": ["TOP CARE (Topco Associates LLC)"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (36800-193-11)  / 20 CAPSULE, LIQUID FILLED in 1 BOTTLE", "package_ndc": "36800-193-11", "marketing_start_date": "20210702"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (36800-193-15)  / 40 CAPSULE, LIQUID FILLED in 1 BOTTLE", "package_ndc": "36800-193-15", "marketing_start_date": "20211229"}, {"sample": false, "description": "80 CAPSULE, LIQUID FILLED in 1 BOTTLE (36800-193-78)", "package_ndc": "36800-193-78", "marketing_start_date": "20210702"}, {"sample": false, "description": "300 CAPSULE, LIQUID FILLED in 1 BOTTLE (36800-193-83)", "package_ndc": "36800-193-83", "marketing_start_date": "20251031"}], "brand_name": "Ibuprofen", "product_id": "36800-193_427b861c-4464-a4b3-e063-6394a90aefb5", "dosage_form": "CAPSULE, LIQUID FILLED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "36800-193", "generic_name": "Ibuprofen", "labeler_name": "TOP CARE (Topco Associates LLC)", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Ibuprofen", "active_ingredients": [{"name": "IBUPROFEN", "strength": "200 mg/1"}], "application_number": "ANDA078682", "marketing_category": "ANDA", "marketing_start_date": "20210702", "listing_expiration_date": "20261231"}