ibuprofen 200

Generic: ibuprofen

Labeler: walgreen company
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name ibuprofen 200
Generic Name ibuprofen
Labeler walgreen company
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

ibuprofen 200 mg/1

Manufacturer
Walgreen Company

Identifiers & Regulatory

Product NDC 0363-1517
Product ID 0363-1517_d7333eba-e5a2-4e80-aa6b-aa0102ebe6d4
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA077349
Listing Expiration 2026-12-31
Marketing Start 2021-10-20

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 03631517
Hyphenated Format 0363-1517

Supplemental Identifiers

RxCUI
310965
UPC
0717917056364
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 200 (source: ndc)
Generic Name ibuprofen (source: ndc)
Application Number ANDA077349 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 200 mg/1
source: ndc
Packaging
  • 1 BOTTLE in 1 CARTON (0363-1517-78) / 100 TABLET, FILM COATED in 1 BOTTLE
source: ndc

Packages (1)

Ingredients (1)

ibuprofen (200 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "d7333eba-e5a2-4e80-aa6b-aa0102ebe6d4", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "upc": ["0717917056364"], "unii": ["WK2XYI10QM"], "rxcui": ["310965"], "spl_set_id": ["49a3d51d-55d1-4b80-ab7b-35c27a937cb9"], "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": ["Walgreen Company"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (0363-1517-78)  / 100 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "0363-1517-78", "marketing_start_date": "20211020"}], "brand_name": "ibuprofen 200", "product_id": "0363-1517_d7333eba-e5a2-4e80-aa6b-aa0102ebe6d4", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "0363-1517", "generic_name": "Ibuprofen", "labeler_name": "Walgreen Company", "product_type": "HUMAN OTC DRUG", "brand_name_base": "ibuprofen 200", "active_ingredients": [{"name": "IBUPROFEN", "strength": "200 mg/1"}], "application_number": "ANDA077349", "marketing_category": "ANDA", "marketing_start_date": "20211020", "listing_expiration_date": "20261231"}