ibuprofen
Generic: ibuprofen
Labeler: kroger companyDrug Facts
Product Profile
Brand Name
ibuprofen
Generic Name
ibuprofen
Labeler
kroger company
Dosage Form
TABLET, FILM COATED
Routes
Active Ingredients
ibuprofen 200 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
30142-517
Product ID
30142-517_d9e7a8c1-51c8-40d2-868f-c9130fb40f45
Product Type
HUMAN OTC DRUG
Marketing Category
ANDA
Application Number
ANDA077349
Listing Expiration
2026-12-31
Marketing Start
2006-04-27
Pharmacologic Class
Established (EPC)
Mechanism of Action
Chemical Structure
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
30142517
Hyphenated Format
30142-517
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
ANDA077349 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 200 mg/1
Packaging
- 1 BOTTLE in 1 CARTON (30142-517-78) / 100 TABLET, FILM COATED in 1 BOTTLE
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "d9e7a8c1-51c8-40d2-868f-c9130fb40f45", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "unii": ["WK2XYI10QM"], "rxcui": ["310965"], "spl_set_id": ["8797f1ba-0df0-4c57-a69b-55aec4d5ed76"], "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": ["Kroger Company"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (30142-517-78) / 100 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "30142-517-78", "marketing_start_date": "20060427"}], "brand_name": "ibuprofen", "product_id": "30142-517_d9e7a8c1-51c8-40d2-868f-c9130fb40f45", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "30142-517", "generic_name": "Ibuprofen", "labeler_name": "Kroger Company", "product_type": "HUMAN OTC DRUG", "brand_name_base": "ibuprofen", "active_ingredients": [{"name": "IBUPROFEN", "strength": "200 mg/1"}], "application_number": "ANDA077349", "marketing_category": "ANDA", "marketing_start_date": "20060427", "listing_expiration_date": "20261231"}