ibuprofen
Generic: ibuprofen
Labeler: p & l development, llcDrug Facts
Product Profile
Brand Name
ibuprofen
Generic Name
ibuprofen
Labeler
p & l development, llc
Dosage Form
CAPSULE, LIQUID FILLED
Routes
Active Ingredients
ibuprofen 200 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
59726-046
Product ID
59726-046_0cccdcc0-9b0b-434e-b693-82924b44f3d9
Product Type
HUMAN OTC DRUG
Marketing Category
ANDA
Application Number
ANDA207753
Marketing Start
2020-12-04
Marketing End
2027-02-01
Pharmacologic Class
Established (EPC)
Mechanism of Action
Chemical Structure
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
59726046
Hyphenated Format
59726-046
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
ANDA207753 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 200 mg/1
Packaging
- 160 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC (59726-046-16)
- 1 BOTTLE, PLASTIC in 1 BOX (59726-046-20) / 20 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC
- 1 BOTTLE, PLASTIC in 1 BOX (59726-046-30) / 30 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC
Packages (3)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "0cccdcc0-9b0b-434e-b693-82924b44f3d9", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "upc": ["0359726745062"], "unii": ["WK2XYI10QM"], "rxcui": ["310964"], "spl_set_id": ["ce215099-91b0-43fd-8ac9-17fe6508842c"], "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": ["P & L Development, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "160 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC (59726-046-16)", "package_ndc": "59726-046-16", "marketing_end_date": "20270201", "marketing_start_date": "20201204"}, {"sample": false, "description": "1 BOTTLE, PLASTIC in 1 BOX (59726-046-20) / 20 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC", "package_ndc": "59726-046-20", "marketing_end_date": "20270201", "marketing_start_date": "20201204"}, {"sample": false, "description": "1 BOTTLE, PLASTIC in 1 BOX (59726-046-30) / 30 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC", "package_ndc": "59726-046-30", "marketing_end_date": "20270201", "marketing_start_date": "20201204"}], "brand_name": "Ibuprofen", "product_id": "59726-046_0cccdcc0-9b0b-434e-b693-82924b44f3d9", "dosage_form": "CAPSULE, LIQUID FILLED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "59726-046", "generic_name": "Ibuprofen", "labeler_name": "P & L Development, LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Ibuprofen", "active_ingredients": [{"name": "IBUPROFEN", "strength": "200 mg/1"}], "application_number": "ANDA207753", "marketing_category": "ANDA", "marketing_end_date": "20270201", "marketing_start_date": "20201204"}