ibuprofen

Generic: ibuprofen

Labeler: publix super markets inc
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name ibuprofen
Generic Name ibuprofen
Labeler publix super markets inc
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

ibuprofen 200 mg/1

Manufacturer
Publix Super Markets Inc

Identifiers & Regulatory

Product NDC 56062-604
Product ID 56062-604_42166a6e-a38b-446b-837e-3cf2e52a8a3d
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA072096
Listing Expiration 2026-12-31
Marketing Start 1988-09-15

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 56062604
Hyphenated Format 56062-604

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 ANDA072096 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 200 mg/1
source: ndc
Packaging
  • 1 BOTTLE in 1 CARTON (56062-604-71) / 50 TABLET, FILM COATED in 1 BOTTLE
  • 1 BOTTLE in 1 CARTON (56062-604-78) / 100 TABLET, FILM COATED in 1 BOTTLE
  • 1 BOTTLE in 1 CARTON (56062-604-85) / 250 TABLET, FILM COATED in 1 BOTTLE
  • 500 TABLET, FILM COATED in 1 BOTTLE (56062-604-90)
source: ndc

Packages (4)

Ingredients (1)

ibuprofen (200 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "42166a6e-a38b-446b-837e-3cf2e52a8a3d", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "unii": ["WK2XYI10QM"], "rxcui": ["310965"], "spl_set_id": ["2dd98554-e434-4617-b789-6ecce7144988"], "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": ["Publix Super Markets Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (56062-604-71)  / 50 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "56062-604-71", "marketing_start_date": "20021226"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (56062-604-78)  / 100 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "56062-604-78", "marketing_start_date": "19880915"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (56062-604-85)  / 250 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "56062-604-85", "marketing_start_date": "20000320"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (56062-604-90)", "package_ndc": "56062-604-90", "marketing_start_date": "20041021"}], "brand_name": "ibuprofen", "product_id": "56062-604_42166a6e-a38b-446b-837e-3cf2e52a8a3d", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "56062-604", "generic_name": "Ibuprofen", "labeler_name": "Publix Super Markets Inc", "product_type": "HUMAN OTC DRUG", "brand_name_base": "ibuprofen", "active_ingredients": [{"name": "IBUPROFEN", "strength": "200 mg/1"}], "application_number": "ANDA072096", "marketing_category": "ANDA", "marketing_start_date": "19880915", "listing_expiration_date": "20261231"}