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 CAPSULE, LIQUID FILLED
Routes
ORAL
Active Ingredients

ibuprofen 200 mg/1

Manufacturer
KROGER COMPANY

Identifiers & Regulatory

Product NDC 30142-053
Product ID 30142-053_f0d5fbf0-cf4f-218d-e053-2a95a90ada47
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA078682
Listing Expiration 2026-12-31
Marketing Start 2019-05-03

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 30142053
Hyphenated Format 30142-053

Supplemental Identifiers

RxCUI
310964
UPC
0041260003837
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 ANDA078682 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 200 mg/1
source: ndc
Packaging
  • 200 CAPSULE, LIQUID FILLED in 1 BOTTLE (30142-053-26)
  • 1 BOTTLE in 1 CARTON (30142-053-82) / 40 CAPSULE, LIQUID FILLED in 1 BOTTLE
  • 1 BOTTLE in 1 CARTON (30142-053-83) / 20 CAPSULE, LIQUID FILLED in 1 BOTTLE
  • 80 CAPSULE, LIQUID FILLED in 1 BOTTLE (30142-053-84)
  • 160 CAPSULE, LIQUID FILLED in 1 BOTTLE (30142-053-85)
source: ndc

Packages (5)

30142-053-26 200 CAPSULE, LIQUID FILLED in 1 BOTTLE (30142-053-26) 30142-053-82 1 BOTTLE in 1 CARTON (30142-053-82) / 40 CAPSULE, LIQUID FILLED in 1 BOTTLE 30142-053-83 1 BOTTLE in 1 CARTON (30142-053-83) / 20 CAPSULE, LIQUID FILLED in 1 BOTTLE 30142-053-84 80 CAPSULE, LIQUID FILLED in 1 BOTTLE (30142-053-84) 30142-053-85 160 CAPSULE, LIQUID FILLED in 1 BOTTLE (30142-053-85)

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": "f0d5fbf0-cf4f-218d-e053-2a95a90ada47", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "upc": ["0041260003837"], "unii": ["WK2XYI10QM"], "rxcui": ["310964"], "spl_set_id": ["3b95dcbf-aef1-44b5-a2c4-5ce93c57ff1d"], "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": "200 CAPSULE, LIQUID FILLED in 1 BOTTLE (30142-053-26)", "package_ndc": "30142-053-26", "marketing_start_date": "20191009"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (30142-053-82)  / 40 CAPSULE, LIQUID FILLED in 1 BOTTLE", "package_ndc": "30142-053-82", "marketing_start_date": "20190503"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (30142-053-83)  / 20 CAPSULE, LIQUID FILLED in 1 BOTTLE", "package_ndc": "30142-053-83", "marketing_start_date": "20190503"}, {"sample": false, "description": "80 CAPSULE, LIQUID FILLED in 1 BOTTLE (30142-053-84)", "package_ndc": "30142-053-84", "marketing_start_date": "20190503"}, {"sample": false, "description": "160 CAPSULE, LIQUID FILLED in 1 BOTTLE (30142-053-85)", "package_ndc": "30142-053-85", "marketing_start_date": "20190503"}], "brand_name": "Ibuprofen", "product_id": "30142-053_f0d5fbf0-cf4f-218d-e053-2a95a90ada47", "dosage_form": "CAPSULE, LIQUID FILLED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "30142-053", "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": "ANDA078682", "marketing_category": "ANDA", "marketing_start_date": "20190503", "listing_expiration_date": "20261231"}