ibuprofen

Generic: ibuprofen

Labeler: walgreens
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name ibuprofen
Generic Name ibuprofen
Labeler walgreens
Dosage Form TABLET
Routes
ORAL
Active Ingredients

ibuprofen 200 mg/1

Manufacturer
WALGREENS

Identifiers & Regulatory

Product NDC 0363-9600
Product ID 0363-9600_13e957be-9a42-aa4e-e063-6394a90a2ae8
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA091239
Listing Expiration 2026-12-31
Marketing Start 2018-12-11

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 03639600
Hyphenated Format 0363-9600

Supplemental Identifiers

RxCUI
310965
UNII
WK2XYI10QM
NUI
N0000000160 M0001335 N0000175722

Packaging Origin

Original Packager
true

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 ANDA091239 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 200 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE, PLASTIC (0363-9600-01)
  • 50 TABLET in 1 BOTTLE, PLASTIC (0363-9600-05)
  • 300 TABLET in 1 BOTTLE, GLASS (0363-9600-31)
  • 24 TABLET in 1 BOTTLE, PLASTIC (0363-9600-42)
  • 500 TABLET in 1 BOTTLE, PLASTIC (0363-9600-50)
source: ndc

Packages (5)

0363-9600-01 100 TABLET in 1 BOTTLE, PLASTIC (0363-9600-01) 0363-9600-05 50 TABLET in 1 BOTTLE, PLASTIC (0363-9600-05) 0363-9600-31 300 TABLET in 1 BOTTLE, GLASS (0363-9600-31) 0363-9600-42 24 TABLET in 1 BOTTLE, PLASTIC (0363-9600-42) 0363-9600-50 500 TABLET in 1 BOTTLE, PLASTIC (0363-9600-50)

Ingredients (1)

ibuprofen (200 mg/1)

Linked Drug Pages (1)

IBUPROFEN ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "13e957be-9a42-aa4e-e063-6394a90a2ae8", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "unii": ["WK2XYI10QM"], "rxcui": ["310965"], "spl_set_id": ["746f79aa-3036-1b9b-e053-2a91aa0a1db6"], "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": ["WALGREENS"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (0363-9600-01)", "package_ndc": "0363-9600-01", "marketing_start_date": "20181211"}, {"sample": false, "description": "50 TABLET in 1 BOTTLE, PLASTIC (0363-9600-05)", "package_ndc": "0363-9600-05", "marketing_start_date": "20181211"}, {"sample": false, "description": "300 TABLET in 1 BOTTLE, GLASS (0363-9600-31)", "package_ndc": "0363-9600-31", "marketing_start_date": "20181211"}, {"sample": false, "description": "24 TABLET in 1 BOTTLE, PLASTIC (0363-9600-42)", "package_ndc": "0363-9600-42", "marketing_start_date": "20181211"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE, PLASTIC (0363-9600-50)", "package_ndc": "0363-9600-50", "marketing_start_date": "20181211"}], "brand_name": "IBUPROFEN", "product_id": "0363-9600_13e957be-9a42-aa4e-e063-6394a90a2ae8", "dosage_form": "TABLET", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "0363-9600", "generic_name": "IBUPROFEN", "labeler_name": "WALGREENS", "product_type": "HUMAN OTC DRUG", "brand_name_base": "IBUPROFEN", "active_ingredients": [{"name": "IBUPROFEN", "strength": "200 mg/1"}], "application_number": "ANDA091239", "marketing_category": "ANDA", "marketing_start_date": "20181211", "listing_expiration_date": "20261231"}