ibuprofen
Generic: ibuprofen
Labeler: proficient rx lpDrug Facts
Product Profile
Brand Name
ibuprofen
Generic Name
ibuprofen
Labeler
proficient rx lp
Dosage Form
TABLET
Routes
Active Ingredients
ibuprofen 800 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
63187-022
Product ID
63187-022_7db62aa5-dd71-4f62-b656-c4df75686f02
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA078558
Listing Expiration
2026-12-31
Marketing Start
2009-11-23
Pharmacologic Class
Established (EPC)
Mechanism of Action
Chemical Structure
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
63187022
Hyphenated Format
63187-022
Supplemental Identifiers
RxCUI
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
ibuprofen (source: ndc)
Generic Name
ibuprofen (source: ndc)
Application Number
ANDA078558 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 800 mg/1
Packaging
- 15 TABLET in 1 BOTTLE (63187-022-15)
- 20 TABLET in 1 BOTTLE (63187-022-20)
- 21 TABLET in 1 BOTTLE (63187-022-21)
- 30 TABLET in 1 BOTTLE (63187-022-30)
- 40 TABLET in 1 BOTTLE (63187-022-40)
- 45 TABLET in 1 BOTTLE (63187-022-45)
- 60 TABLET in 1 BOTTLE (63187-022-60)
- 120 TABLET in 1 BOTTLE (63187-022-72)
- 90 TABLET in 1 BOTTLE (63187-022-90)
Packages (9)
63187-022-15
15 TABLET in 1 BOTTLE (63187-022-15)
63187-022-20
20 TABLET in 1 BOTTLE (63187-022-20)
63187-022-21
21 TABLET in 1 BOTTLE (63187-022-21)
63187-022-30
30 TABLET in 1 BOTTLE (63187-022-30)
63187-022-40
40 TABLET in 1 BOTTLE (63187-022-40)
63187-022-45
45 TABLET in 1 BOTTLE (63187-022-45)
63187-022-60
60 TABLET in 1 BOTTLE (63187-022-60)
63187-022-72
120 TABLET in 1 BOTTLE (63187-022-72)
63187-022-90
90 TABLET in 1 BOTTLE (63187-022-90)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "7db62aa5-dd71-4f62-b656-c4df75686f02", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "unii": ["WK2XYI10QM"], "rxcui": ["197805", "197806", "197807"], "spl_set_id": ["e23eb275-ce0c-40ec-b809-a48c5e46c7ec"], "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 (63187-022-15)", "package_ndc": "63187-022-15", "marketing_start_date": "20140501"}, {"sample": false, "description": "20 TABLET in 1 BOTTLE (63187-022-20)", "package_ndc": "63187-022-20", "marketing_start_date": "20160901"}, {"sample": false, "description": "21 TABLET in 1 BOTTLE (63187-022-21)", "package_ndc": "63187-022-21", "marketing_start_date": "20170901"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (63187-022-30)", "package_ndc": "63187-022-30", "marketing_start_date": "20140501"}, {"sample": false, "description": "40 TABLET in 1 BOTTLE (63187-022-40)", "package_ndc": "63187-022-40", "marketing_start_date": "20140501"}, {"sample": false, "description": "45 TABLET in 1 BOTTLE (63187-022-45)", "package_ndc": "63187-022-45", "marketing_start_date": "20140501"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (63187-022-60)", "package_ndc": "63187-022-60", "marketing_start_date": "20140501"}, {"sample": false, "description": "120 TABLET in 1 BOTTLE (63187-022-72)", "package_ndc": "63187-022-72", "marketing_start_date": "20140501"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (63187-022-90)", "package_ndc": "63187-022-90", "marketing_start_date": "20140501"}], "brand_name": "Ibuprofen", "product_id": "63187-022_7db62aa5-dd71-4f62-b656-c4df75686f02", "dosage_form": "TABLET", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "63187-022", "generic_name": "Ibuprofen", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ibuprofen", "active_ingredients": [{"name": "IBUPROFEN", "strength": "800 mg/1"}], "application_number": "ANDA078558", "marketing_category": "ANDA", "marketing_start_date": "20091123", "listing_expiration_date": "20261231"}