ibu
Generic: ibuprofen
Labeler: proficient rx lpDrug Facts
Product Profile
Brand Name
ibu
Generic Name
ibuprofen
Labeler
proficient rx lp
Dosage Form
TABLET
Routes
Active Ingredients
ibuprofen 600 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
63187-614
Product ID
63187-614_144ceffa-24aa-4423-ba09-1a6fa5c0d5cf
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)
Mechanism of Action
Chemical Structure
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
63187614
Hyphenated Format
63187-614
Supplemental Identifiers
RxCUI
UPC
UNII
NUI
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
source: ndc
Resolved Composition
Strengths
- 600 mg/1
Packaging
- 15 TABLET in 1 BOTTLE (63187-614-15)
- 20 TABLET in 1 BOTTLE (63187-614-20)
- 21 TABLET in 1 BOTTLE (63187-614-21)
- 28 TABLET in 1 BOTTLE (63187-614-28)
- 30 TABLET in 1 BOTTLE (63187-614-30)
- 40 TABLET in 1 BOTTLE (63187-614-40)
- 42 TABLET in 1 BOTTLE (63187-614-42)
- 45 TABLET in 1 BOTTLE (63187-614-45)
- 60 TABLET in 1 BOTTLE (63187-614-60)
- 90 TABLET in 1 BOTTLE (63187-614-90)
Packages (10)
63187-614-15
15 TABLET in 1 BOTTLE (63187-614-15)
63187-614-20
20 TABLET in 1 BOTTLE (63187-614-20)
63187-614-21
21 TABLET in 1 BOTTLE (63187-614-21)
63187-614-28
28 TABLET in 1 BOTTLE (63187-614-28)
63187-614-30
30 TABLET in 1 BOTTLE (63187-614-30)
63187-614-40
40 TABLET in 1 BOTTLE (63187-614-40)
63187-614-42
42 TABLET in 1 BOTTLE (63187-614-42)
63187-614-45
45 TABLET in 1 BOTTLE (63187-614-45)
63187-614-60
60 TABLET in 1 BOTTLE (63187-614-60)
63187-614-90
90 TABLET in 1 BOTTLE (63187-614-90)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "144ceffa-24aa-4423-ba09-1a6fa5c0d5cf", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "upc": ["0363187614300"], "unii": ["WK2XYI10QM"], "rxcui": ["197806", "206913"], "spl_set_id": ["a7098fa1-b5ae-485e-ada9-64154f81fb6a"], "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": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "15 TABLET in 1 BOTTLE (63187-614-15)", "package_ndc": "63187-614-15", "marketing_start_date": "20160101"}, {"sample": false, "description": "20 TABLET in 1 BOTTLE (63187-614-20)", "package_ndc": "63187-614-20", "marketing_start_date": "20170301"}, {"sample": false, "description": "21 TABLET in 1 BOTTLE (63187-614-21)", "package_ndc": "63187-614-21", "marketing_start_date": "20251211"}, {"sample": false, "description": "28 TABLET in 1 BOTTLE (63187-614-28)", "package_ndc": "63187-614-28", "marketing_start_date": "20191001"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (63187-614-30)", "package_ndc": "63187-614-30", "marketing_start_date": "20160101"}, {"sample": false, "description": "40 TABLET in 1 BOTTLE (63187-614-40)", "package_ndc": "63187-614-40", "marketing_start_date": "20170601"}, {"sample": false, "description": "42 TABLET in 1 BOTTLE (63187-614-42)", "package_ndc": "63187-614-42", "marketing_start_date": "20200221"}, {"sample": false, "description": "45 TABLET in 1 BOTTLE (63187-614-45)", "package_ndc": "63187-614-45", "marketing_start_date": "20160101"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (63187-614-60)", "package_ndc": "63187-614-60", "marketing_start_date": "20160101"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (63187-614-90)", "package_ndc": "63187-614-90", "marketing_start_date": "20160101"}], "brand_name": "IBU", "product_id": "63187-614_144ceffa-24aa-4423-ba09-1a6fa5c0d5cf", "dosage_form": "TABLET", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "63187-614", "generic_name": "Ibuprofen", "labeler_name": "Proficient Rx LP", "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"}