ibuprofen

Generic: ibuprofen

Labeler: hyvee inc
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name ibuprofen
Generic Name ibuprofen
Labeler hyvee inc
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

ibuprofen 200 mg/1

Manufacturer
HyVee Inc

Identifiers & Regulatory

Product NDC 42507-399
Product ID 42507-399_00024dd6-9c20-45a2-a867-6e1c5353eaa1
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA072096
Listing Expiration 2027-12-31
Marketing Start 2026-01-28

Pharmacologic Class

Established (EPC)
nonsteroidal anti-inflammatory drug [epc]
Mechanism of Action
cyclooxygenase inhibitors [moa]
Chemical Structure
anti-inflammatory agents, non-steroidal [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 42507399
Hyphenated Format 42507-399

Supplemental Identifiers

RxCUI
310965
UNII
WK2XYI10QM
NUI
N0000000160 M0001335 N0000175722

Packaging Origin

Original Packager
true

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 ANDA072096 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 200 mg/1
source: ndc
Packaging
  • 250 TABLET, FILM COATED in 1 BOTTLE (42507-399-85)
source: ndc

Packages (1)

42507-399-85 250 TABLET, FILM COATED in 1 BOTTLE (42507-399-85)

Ingredients (1)

ibuprofen (200 mg/1)

Linked Drug Pages (1)

ibuprofen ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "00024dd6-9c20-45a2-a867-6e1c5353eaa1", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "unii": ["WK2XYI10QM"], "rxcui": ["310965"], "spl_set_id": ["5233c409-3743-4312-9f75-14ded6755b5c"], "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": ["HyVee Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "250 TABLET, FILM COATED in 1 BOTTLE (42507-399-85)", "package_ndc": "42507-399-85", "marketing_start_date": "20260128"}], "brand_name": "ibuprofen", "product_id": "42507-399_00024dd6-9c20-45a2-a867-6e1c5353eaa1", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "42507-399", "generic_name": "Ibuprofen", "labeler_name": "HyVee Inc", "product_type": "HUMAN OTC DRUG", "brand_name_base": "ibuprofen", "active_ingredients": [{"name": "IBUPROFEN", "strength": "200 mg/1"}], "application_number": "ANDA072096", "marketing_category": "ANDA", "marketing_start_date": "20260128", "listing_expiration_date": "20271231"}