ibuprofen
Generic: ibuprofen
Labeler: shield pharmaceuticals corpDrug Facts
Product Profile
Brand Name
ibuprofen
Generic Name
ibuprofen
Labeler
shield pharmaceuticals corp
Dosage Form
TABLET, COATED
Routes
Active Ingredients
ibuprofen 200 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
83059-0020
Product ID
83059-0020_458bb39e-2e8a-b4b4-e063-6394a90ae867
Product Type
HUMAN OTC DRUG
Marketing Category
ANDA
Application Number
ANDA207095
Listing Expiration
2026-12-31
Marketing Start
2024-01-26
Pharmacologic Class
Established (EPC)
Mechanism of Action
Chemical Structure
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
830590020
Hyphenated Format
83059-0020
Supplemental Identifiers
RxCUI
UNII
NUI
Packaging Origin
Original Packager
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
ANDA207095 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 200 mg/1
Packaging
- 1 BOTTLE in 1 CARTON (83059-0020-4) / 40 TABLET, COATED in 1 BOTTLE
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "458bb39e-2e8a-b4b4-e063-6394a90ae867", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "unii": ["WK2XYI10QM"], "rxcui": ["310965"], "spl_set_id": ["fc6c29b4-f1b3-4cfe-8c96-564d083be39c"], "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": ["Shield Pharmaceuticals Corp"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (83059-0020-4) / 40 TABLET, COATED in 1 BOTTLE", "package_ndc": "83059-0020-4", "marketing_start_date": "20240126"}], "brand_name": "Ibuprofen", "product_id": "83059-0020_458bb39e-2e8a-b4b4-e063-6394a90ae867", "dosage_form": "TABLET, COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "83059-0020", "generic_name": "Ibuprofen", "labeler_name": "Shield Pharmaceuticals Corp", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Ibuprofen", "active_ingredients": [{"name": "IBUPROFEN", "strength": "200 mg/1"}], "application_number": "ANDA207095", "marketing_category": "ANDA", "marketing_start_date": "20240126", "listing_expiration_date": "20261231"}