ibuprofen
Generic: ibuprofen
Labeler: aaa pharmaceutical, inc.Drug Facts
Product Profile
Brand Name
ibuprofen
Generic Name
ibuprofen
Labeler
aaa pharmaceutical, inc.
Dosage Form
TABLET, COATED
Routes
Active Ingredients
ibuprofen 200 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
57344-811
Product ID
57344-811_37ca1bc2-6519-4a6c-e063-6394a90a3018
Product Type
HUMAN OTC DRUG
Marketing Category
ANDA
Application Number
ANDA202312
Listing Expiration
2026-12-31
Marketing Start
2020-02-01
Pharmacologic Class
Established (EPC)
Mechanism of Action
Chemical Structure
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
57344811
Hyphenated Format
57344-811
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
ANDA202312 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 200 mg/1
Packaging
- 1 BOTTLE, PLASTIC in 1 CARTON (57344-811-03) / 100 TABLET, 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": "37ca1bc2-6519-4a6c-e063-6394a90a3018", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "upc": ["0099581910860"], "unii": ["WK2XYI10QM"], "rxcui": ["310965"], "spl_set_id": ["78cf5df8-392b-4a4e-b424-af765a6defdf"], "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": ["AAA Pharmaceutical, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (57344-811-03) / 100 TABLET, COATED in 1 BOTTLE, PLASTIC", "package_ndc": "57344-811-03", "marketing_start_date": "20200201"}], "brand_name": "Ibuprofen", "product_id": "57344-811_37ca1bc2-6519-4a6c-e063-6394a90a3018", "dosage_form": "TABLET, COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "57344-811", "generic_name": "Ibuprofen", "labeler_name": "AAA Pharmaceutical, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Ibuprofen", "active_ingredients": [{"name": "IBUPROFEN", "strength": "200 mg/1"}], "application_number": "ANDA202312", "marketing_category": "ANDA", "marketing_start_date": "20200201", "listing_expiration_date": "20261231"}