ibu

Generic: ibuprofen

Labeler: nucare pharmaceuticals inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name ibu
Generic Name ibuprofen
Labeler nucare pharmaceuticals inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

ibuprofen 600 mg/1

Manufacturer
NuCare Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 66267-964
Product ID 66267-964_1fa7d49f-eae6-218c-e063-6294a90a0eb8
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA075682
Listing Expiration 2026-12-31
Marketing Start 2008-11-20

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 66267964
Hyphenated Format 66267-964

Supplemental Identifiers

RxCUI
197806 206913
UNII
WK2XYI10QM
NUI
N0000000160 M0001335 N0000175722

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 ibu (source: ndc)
Generic Name ibuprofen (source: ndc)
Application Number ANDA075682 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 600 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (66267-964-00)
source: ndc

Packages (1)

66267-964-00 100 TABLET in 1 BOTTLE (66267-964-00)

Ingredients (1)

ibuprofen (600 mg/1)

Linked Drug Pages (1)

IBU ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "1fa7d49f-eae6-218c-e063-6294a90a0eb8", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "unii": ["WK2XYI10QM"], "rxcui": ["197806", "206913"], "spl_set_id": ["575c275c-3e1a-0572-e053-2991aa0adabd"], "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": ["NuCare Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (66267-964-00)", "package_ndc": "66267-964-00", "marketing_start_date": "20170822"}], "brand_name": "IBU", "product_id": "66267-964_1fa7d49f-eae6-218c-e063-6294a90a0eb8", "dosage_form": "TABLET", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "66267-964", "generic_name": "Ibuprofen", "labeler_name": "NuCare Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "IBU", "active_ingredients": [{"name": "IBUPROFEN", "strength": "600 mg/1"}], "application_number": "ANDA075682", "marketing_category": "ANDA", "marketing_start_date": "20081120", "listing_expiration_date": "20261231"}