dye free ibuprofen (70729-002)

Drug Facts

Product Profile

Brand Name dye free ibuprofen

Generic Name ibuprofen

Labeler breeden brothers, llc

Dosage Form TABLET

Routes

ORAL

Active Ingredients

ibuprofen 200 mg/1

Manufacturer

Breeden Brothers, LLC

Identifiers & Regulatory

Product NDC 70729-002

Product ID 70729-002_e7bbd188-5e3e-4f1c-96d8-53f6de4b3120

Product Type HUMAN OTC DRUG

Marketing Category ANDA

Application Number ANDA075139

Listing Expiration 2026-12-31

Marketing Start 1999-03-01

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 70729002

Hyphenated Format 70729-002

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 dye free ibuprofen (source: ndc)

Generic Name ibuprofen (source: ndc)

Application Number ANDA075139 (source: ndc)

Routes

ORAL

source: ndc

Resolved Composition

Strengths

200 mg/1

source: ndc

Packaging

24 TABLET in 1 BOTTLE (70729-002-24)
50 TABLET in 1 BOTTLE (70729-002-50)

source: ndc

Packages (2)

70729-002-24 24 TABLET in 1 BOTTLE (70729-002-24) 70729-002-50 50 TABLET in 1 BOTTLE (70729-002-50)

Ingredients (1)

ibuprofen (200 mg/1)

Linked Drug Pages (1)

Dye Free Ibuprofen ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload

{"route": ["ORAL"], "spl_id": "e7bbd188-5e3e-4f1c-96d8-53f6de4b3120", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "unii": ["WK2XYI10QM"], "rxcui": ["310965"], "spl_set_id": ["ba106f6f-2c6b-4c98-a10e-d27622b08b25"], "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": ["Breeden Brothers, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "24 TABLET in 1 BOTTLE (70729-002-24)", "package_ndc": "70729-002-24", "marketing_start_date": "19990301"}, {"sample": false, "description": "50 TABLET in 1 BOTTLE (70729-002-50)", "package_ndc": "70729-002-50", "marketing_start_date": "19990301"}], "brand_name": "Dye Free Ibuprofen", "product_id": "70729-002_e7bbd188-5e3e-4f1c-96d8-53f6de4b3120", "dosage_form": "TABLET", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "70729-002", "generic_name": "Ibuprofen", "labeler_name": "Breeden Brothers, LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Dye Free Ibuprofen", "active_ingredients": [{"name": "IBUPROFEN", "strength": "200 mg/1"}], "application_number": "ANDA075139", "marketing_category": "ANDA", "marketing_start_date": "19990301", "listing_expiration_date": "20261231"}