ibuprofen

Generic: ibuprofen

Labeler: a-s medication solutions
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name ibuprofen
Generic Name ibuprofen
Labeler a-s medication solutions
Dosage Form TABLET
Routes
ORAL
Active Ingredients

ibuprofen 600 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-5433
Product ID 50090-5433_31988d3c-1f44-4f32-b838-1a54b3d1af9a
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA213794
Listing Expiration 2026-12-31
Marketing Start 2020-05-08

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 500905433
Hyphenated Format 50090-5433

Supplemental Identifiers

RxCUI
197806
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 ANDA213794 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 600 mg/1
source: ndc
Packaging
  • 15 TABLET in 1 BOTTLE (50090-5433-0)
  • 21 TABLET in 1 BOTTLE (50090-5433-1)
  • 28 TABLET in 1 BOTTLE (50090-5433-4)
  • 90 TABLET in 1 BOTTLE (50090-5433-5)
source: ndc

Packages (4)

Ingredients (1)

ibuprofen (600 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "31988d3c-1f44-4f32-b838-1a54b3d1af9a", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "unii": ["WK2XYI10QM"], "rxcui": ["197806"], "spl_set_id": ["8d5f7d2a-af48-4d47-8bf5-48f01c092d24"], "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": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "15 TABLET in 1 BOTTLE (50090-5433-0)", "package_ndc": "50090-5433-0", "marketing_start_date": "20250717"}, {"sample": false, "description": "21 TABLET in 1 BOTTLE (50090-5433-1)", "package_ndc": "50090-5433-1", "marketing_start_date": "20210118"}, {"sample": false, "description": "28 TABLET in 1 BOTTLE (50090-5433-4)", "package_ndc": "50090-5433-4", "marketing_start_date": "20210118"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (50090-5433-5)", "package_ndc": "50090-5433-5", "marketing_start_date": "20210118"}], "brand_name": "Ibuprofen", "product_id": "50090-5433_31988d3c-1f44-4f32-b838-1a54b3d1af9a", "dosage_form": "TABLET", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "50090-5433", "generic_name": "Ibuprofen", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ibuprofen", "active_ingredients": [{"name": "IBUPROFEN", "strength": "600 mg/1"}], "application_number": "ANDA213794", "marketing_category": "ANDA", "marketing_start_date": "20200508", "listing_expiration_date": "20261231"}