ibuprofen
Generic: ibuprofen
Labeler: pd-rx pharmaceuticals, inc.Drug Facts
Product Profile
Brand Name
ibuprofen
Generic Name
ibuprofen
Labeler
pd-rx pharmaceuticals, inc.
Dosage Form
TABLET, FILM COATED
Routes
Active Ingredients
ibuprofen 800 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
72789-186
Product ID
72789-186_34178401-0edc-512f-e063-6294a90ab88a
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA078329
Listing Expiration
2026-12-31
Marketing Start
2020-08-21
Pharmacologic Class
Established (EPC)
Mechanism of Action
Chemical Structure
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
72789186
Hyphenated Format
72789-186
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
ibuprofen (source: ndc)
Generic Name
ibuprofen (source: ndc)
Application Number
ANDA078329 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 800 mg/1
Packaging
- 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-186-30)
- 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-186-60)
- 500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-186-82)
- 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-186-90)
Packages (4)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "34178401-0edc-512f-e063-6294a90ab88a", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "upc": ["0372789186825", "0372789187822", "0372789185309"], "unii": ["WK2XYI10QM"], "rxcui": ["197805", "197806", "197807"], "spl_set_id": ["3732defa-67c2-4b84-8a84-4bbc27b6cb24"], "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": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-186-30)", "package_ndc": "72789-186-30", "marketing_start_date": "20210518"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-186-60)", "package_ndc": "72789-186-60", "marketing_start_date": "20210518"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-186-82)", "package_ndc": "72789-186-82", "marketing_start_date": "20210511"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-186-90)", "package_ndc": "72789-186-90", "marketing_start_date": "20210518"}], "brand_name": "Ibuprofen", "product_id": "72789-186_34178401-0edc-512f-e063-6294a90ab88a", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "72789-186", "generic_name": "Ibuprofen", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ibuprofen", "active_ingredients": [{"name": "IBUPROFEN", "strength": "800 mg/1"}], "application_number": "ANDA078329", "marketing_category": "ANDA", "marketing_start_date": "20200821", "listing_expiration_date": "20261231"}