ibuprofen

Generic: ibuprofen

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

Drug Facts

Product Profile

Brand Name ibuprofen
Generic Name ibuprofen
Labeler preferred pharmaceuticals, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

ibuprofen 600 mg/1

Manufacturer
Preferred Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 68788-9111
Product ID 68788-9111_8e207ebc-b100-4b1f-ab43-b869b14065ba
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 687889111
Hyphenated Format 68788-9111

Supplemental Identifiers

RxCUI
197805 197806 197807
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 ibuprofen (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 (68788-9111-1)
  • 20 TABLET in 1 BOTTLE (68788-9111-2)
  • 30 TABLET in 1 BOTTLE (68788-9111-3)
  • 50 TABLET in 1 BOTTLE (68788-9111-5)
  • 60 TABLET in 1 BOTTLE (68788-9111-6)
  • 21 TABLET in 1 BOTTLE (68788-9111-7)
  • 120 TABLET in 1 BOTTLE (68788-9111-8)
  • 90 TABLET in 1 BOTTLE (68788-9111-9)
source: ndc

Packages (8)

68788-9111-1 100 TABLET in 1 BOTTLE (68788-9111-1) 68788-9111-2 20 TABLET in 1 BOTTLE (68788-9111-2) 68788-9111-3 30 TABLET in 1 BOTTLE (68788-9111-3) 68788-9111-5 50 TABLET in 1 BOTTLE (68788-9111-5) 68788-9111-6 60 TABLET in 1 BOTTLE (68788-9111-6) 68788-9111-7 21 TABLET in 1 BOTTLE (68788-9111-7) 68788-9111-8 120 TABLET in 1 BOTTLE (68788-9111-8) 68788-9111-9 90 TABLET in 1 BOTTLE (68788-9111-9)

Ingredients (1)

ibuprofen (600 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": "8e207ebc-b100-4b1f-ab43-b869b14065ba", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "unii": ["WK2XYI10QM"], "rxcui": ["197805", "197806", "197807"], "spl_set_id": ["72ec2491-924d-460f-9510-62d624d54b59"], "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": ["Preferred Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (68788-9111-1)", "package_ndc": "68788-9111-1", "marketing_start_date": "20081120"}, {"sample": false, "description": "20 TABLET in 1 BOTTLE (68788-9111-2)", "package_ndc": "68788-9111-2", "marketing_start_date": "20081120"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (68788-9111-3)", "package_ndc": "68788-9111-3", "marketing_start_date": "20081120"}, {"sample": false, "description": "50 TABLET in 1 BOTTLE (68788-9111-5)", "package_ndc": "68788-9111-5", "marketing_start_date": "20081120"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (68788-9111-6)", "package_ndc": "68788-9111-6", "marketing_start_date": "20081120"}, {"sample": false, "description": "21 TABLET in 1 BOTTLE (68788-9111-7)", "package_ndc": "68788-9111-7", "marketing_start_date": "20081120"}, {"sample": false, "description": "120 TABLET in 1 BOTTLE (68788-9111-8)", "package_ndc": "68788-9111-8", "marketing_start_date": "20081120"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (68788-9111-9)", "package_ndc": "68788-9111-9", "marketing_start_date": "20081120"}], "brand_name": "Ibuprofen", "product_id": "68788-9111_8e207ebc-b100-4b1f-ab43-b869b14065ba", "dosage_form": "TABLET", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "68788-9111", "generic_name": "Ibuprofen", "labeler_name": "Preferred Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ibuprofen", "active_ingredients": [{"name": "IBUPROFEN", "strength": "600 mg/1"}], "application_number": "ANDA075682", "marketing_category": "ANDA", "marketing_start_date": "20081120", "listing_expiration_date": "20261231"}