ibuprofen

Generic: ibuprofen

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

Drug Facts

Product Profile

Brand Name ibuprofen
Generic Name ibuprofen
Labeler kroger company
Dosage Form TABLET, COATED
Routes
ORAL
Active Ingredients

ibuprofen 200 mg/1

Manufacturer
Kroger Company

Identifiers & Regulatory

Product NDC 41226-600
Product ID 41226-600_3f8861cb-53a2-83f7-e063-6394a90a3879
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA091239
Listing Expiration 2026-12-31
Marketing Start 2021-06-12

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 41226600
Hyphenated Format 41226-600

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
  • 1 BOTTLE in 1 CARTON (41226-600-01) / 100 TABLET, COATED in 1 BOTTLE
  • 1 BOTTLE in 1 CARTON (41226-600-42) / 24 TABLET, COATED in 1 BOTTLE
  • 500 TABLET, COATED in 1 BOTTLE (41226-600-50)
source: ndc

Packages (3)

41226-600-01 1 BOTTLE in 1 CARTON (41226-600-01) / 100 TABLET, COATED in 1 BOTTLE 41226-600-42 1 BOTTLE in 1 CARTON (41226-600-42) / 24 TABLET, COATED in 1 BOTTLE 41226-600-50 500 TABLET, COATED in 1 BOTTLE (41226-600-50)

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": "3f8861cb-53a2-83f7-e063-6394a90a3879", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "unii": ["WK2XYI10QM"], "rxcui": ["310965"], "spl_set_id": ["bc173f1b-2e44-2c2e-e053-2a95a90a89c4"], "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": ["Kroger Company"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (41226-600-01)  / 100 TABLET, COATED in 1 BOTTLE", "package_ndc": "41226-600-01", "marketing_start_date": "20210612"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (41226-600-42)  / 24 TABLET, COATED in 1 BOTTLE", "package_ndc": "41226-600-42", "marketing_start_date": "20210612"}, {"sample": false, "description": "500 TABLET, COATED in 1 BOTTLE (41226-600-50)", "package_ndc": "41226-600-50", "marketing_start_date": "20210612"}], "brand_name": "IBUPROFEN", "product_id": "41226-600_3f8861cb-53a2-83f7-e063-6394a90a3879", "dosage_form": "TABLET, COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "41226-600", "generic_name": "IBUPROFEN", "labeler_name": "Kroger Company", "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": "20210612", "listing_expiration_date": "20261231"}