ibuprofen
Generic: ibuprofen
Labeler: chain drug consortiumDrug Facts
Product Profile
Brand Name
ibuprofen
Generic Name
ibuprofen
Labeler
chain drug consortium
Dosage Form
TABLET, FILM COATED
Routes
Active Ingredients
ibuprofen 200 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
68016-645
Product ID
68016-645_d2415143-02bb-4721-9d15-68833cbc7efb
Product Type
HUMAN OTC DRUG
Marketing Category
ANDA
Application Number
ANDA075010
Marketing Start
1988-05-24
Marketing End
2026-08-31
Pharmacologic Class
Established (EPC)
Mechanism of Action
Chemical Structure
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
68016645
Hyphenated Format
68016-645
Supplemental Identifiers
RxCUI
UPC
UNII
NUI
Packaging Origin
Original Packager
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
ibuprofen (source: ndc)
Generic Name
ibuprofen (source: ndc)
Application Number
ANDA075010 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 200 mg/1
Packaging
- 1 BOTTLE, PLASTIC in 1 CARTON (68016-645-08) / 24 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
- 1 BOTTLE, PLASTIC in 1 CARTON (68016-645-12) / 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
- 1 BOTTLE, PLASTIC in 1 CARTON (68016-645-15) / 50 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
Packages (3)
68016-645-08
1 BOTTLE, PLASTIC in 1 CARTON (68016-645-08) / 24 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
68016-645-12
1 BOTTLE, PLASTIC in 1 CARTON (68016-645-12) / 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
68016-645-15
1 BOTTLE, PLASTIC in 1 CARTON (68016-645-15) / 50 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "d2415143-02bb-4721-9d15-68833cbc7efb", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "upc": ["0840986031502"], "unii": ["WK2XYI10QM"], "rxcui": ["310965"], "spl_set_id": ["409941dc-9fd3-4475-bc6c-defe3cfbc61a"], "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": ["Chain Drug Consortium"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (68016-645-08) / 24 TABLET, FILM COATED in 1 BOTTLE, PLASTIC", "package_ndc": "68016-645-08", "marketing_end_date": "20260831", "marketing_start_date": "19880524"}, {"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (68016-645-12) / 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC", "package_ndc": "68016-645-12", "marketing_end_date": "20260831", "marketing_start_date": "19880524"}, {"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (68016-645-15) / 50 TABLET, FILM COATED in 1 BOTTLE, PLASTIC", "package_ndc": "68016-645-15", "marketing_end_date": "20260831", "marketing_start_date": "19880524"}], "brand_name": "Ibuprofen", "product_id": "68016-645_d2415143-02bb-4721-9d15-68833cbc7efb", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "68016-645", "generic_name": "Ibuprofen", "labeler_name": "Chain Drug Consortium", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Ibuprofen", "active_ingredients": [{"name": "IBUPROFEN", "strength": "200 mg/1"}], "application_number": "ANDA075010", "marketing_category": "ANDA", "marketing_end_date": "20260831", "marketing_start_date": "19880524"}