ibuprofen
Generic: ibuprofen
Labeler: chain drug marketing association incDrug Facts
Product Profile
Brand Name
ibuprofen
Generic Name
ibuprofen
Labeler
chain drug marketing association inc
Dosage Form
TABLET, FILM COATED
Routes
Active Ingredients
ibuprofen 200 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
63868-979
Product ID
63868-979_17c41cdc-d6d0-40cf-8ac3-ef7ba162b9ba
Product Type
HUMAN OTC DRUG
Marketing Category
ANDA
Application Number
ANDA075010
Marketing Start
1988-05-24
Marketing End
2028-02-28
Pharmacologic Class
Established (EPC)
Mechanism of Action
Chemical Structure
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
63868979
Hyphenated Format
63868-979
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 (63868-979-10) / 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
- 1 BOTTLE, PLASTIC in 1 CARTON (63868-979-24) / 24 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
- 1 BOTTLE, PLASTIC in 1 CARTON (63868-979-50) / 50 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
Packages (3)
63868-979-10
1 BOTTLE, PLASTIC in 1 CARTON (63868-979-10) / 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
63868-979-24
1 BOTTLE, PLASTIC in 1 CARTON (63868-979-24) / 24 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
63868-979-50
1 BOTTLE, PLASTIC in 1 CARTON (63868-979-50) / 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": "17c41cdc-d6d0-40cf-8ac3-ef7ba162b9ba", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "upc": ["0635515980761"], "unii": ["WK2XYI10QM"], "rxcui": ["310965"], "spl_set_id": ["6521bc47-4d9c-4a5b-b109-3841f3be4b6c"], "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 MARKETING ASSOCIATION INC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (63868-979-10) / 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC", "package_ndc": "63868-979-10", "marketing_end_date": "20280228", "marketing_start_date": "19880524"}, {"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (63868-979-24) / 24 TABLET, FILM COATED in 1 BOTTLE, PLASTIC", "package_ndc": "63868-979-24", "marketing_end_date": "20280228", "marketing_start_date": "19880524"}, {"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (63868-979-50) / 50 TABLET, FILM COATED in 1 BOTTLE, PLASTIC", "package_ndc": "63868-979-50", "marketing_end_date": "20280228", "marketing_start_date": "19880524"}], "brand_name": "Ibuprofen", "product_id": "63868-979_17c41cdc-d6d0-40cf-8ac3-ef7ba162b9ba", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "63868-979", "generic_name": "Ibuprofen", "labeler_name": "CHAIN DRUG MARKETING ASSOCIATION INC", "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": "20280228", "marketing_start_date": "19880524"}