ibuprofen
Generic: ibuprofen
Labeler: contract pharmacal corp.Drug Facts
Product Profile
Brand Name
ibuprofen
Generic Name
ibuprofen
Labeler
contract pharmacal corp.
Dosage Form
TABLET
Routes
Active Ingredients
ibuprofen 200 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
10267-3852
Product ID
10267-3852_77cf0092-7436-14ba-e053-2991aa0ac112
Product Type
HUMAN OTC DRUG
Marketing Category
ANDA
Application Number
ANDA071265
Listing Expiration
2026-12-31
Marketing Start
2014-01-15
Pharmacologic Class
Established (EPC)
Mechanism of Action
Chemical Structure
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
102673852
Hyphenated Format
10267-3852
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
ANDA071265 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 200 mg/1
Packaging
- 250 TABLET in 1 BOTTLE (10267-3852-2)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "77cf0092-7436-14ba-e053-2991aa0ac112", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "upc": ["0310267390920", "0310267385223"], "unii": ["WK2XYI10QM"], "rxcui": ["310965"], "spl_set_id": ["237bcb87-64a0-415b-bd53-e9d3b8bf33b6"], "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": ["Contract Pharmacal Corp."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "250 TABLET in 1 BOTTLE (10267-3852-2)", "package_ndc": "10267-3852-2", "marketing_start_date": "20140115"}], "brand_name": "ibuprofen", "product_id": "10267-3852_77cf0092-7436-14ba-e053-2991aa0ac112", "dosage_form": "TABLET", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "10267-3852", "generic_name": "ibuprofen", "labeler_name": "Contract Pharmacal Corp.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "ibuprofen", "active_ingredients": [{"name": "IBUPROFEN", "strength": "200 mg/1"}], "application_number": "ANDA071265", "marketing_category": "ANDA", "marketing_start_date": "20140115", "listing_expiration_date": "20261231"}