ibuprofen
Generic: ibuprofen
Labeler: rite aid corporationDrug Facts
Product Profile
Brand Name
ibuprofen
Generic Name
ibuprofen
Labeler
rite aid corporation
Dosage Form
TABLET, FILM COATED
Routes
Active Ingredients
ibuprofen 200 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
11822-0291
Product ID
11822-0291_b7b180f9-803d-4ffc-b9a4-384fee40cf4f
Product Type
HUMAN OTC DRUG
Marketing Category
ANDA
Application Number
ANDA075010
Listing Expiration
2026-12-31
Marketing Start
1988-05-24
Pharmacologic Class
Established (EPC)
Mechanism of Action
Chemical Structure
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
118220291
Hyphenated Format
11822-0291
Supplemental Identifiers
RxCUI
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 (11822-0291-2) / 12 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "b7b180f9-803d-4ffc-b9a4-384fee40cf4f", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "unii": ["WK2XYI10QM"], "rxcui": ["310965"], "spl_set_id": ["d9e698f3-c450-4eaa-9cfd-6f48c2656081"], "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": ["Rite Aid Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (11822-0291-2) / 12 TABLET, FILM COATED in 1 BOTTLE, PLASTIC", "package_ndc": "11822-0291-2", "marketing_start_date": "19880524"}], "brand_name": "Ibuprofen", "product_id": "11822-0291_b7b180f9-803d-4ffc-b9a4-384fee40cf4f", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "11822-0291", "generic_name": "Ibuprofen", "labeler_name": "Rite Aid Corporation", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Ibuprofen", "active_ingredients": [{"name": "IBUPROFEN", "strength": "200 mg/1"}], "application_number": "ANDA075010", "marketing_category": "ANDA", "marketing_start_date": "19880524", "listing_expiration_date": "20261231"}