ibuprofen, diphenhydramine hcl (11673-225)

Drug Facts

Product Profile

Brand Name ibuprofen, diphenhydramine hcl

Generic Name ibuprofen, diphenhydramine hcl

Labeler target corporation

Dosage Form CAPSULE, LIQUID FILLED

Routes

ORAL

Active Ingredients

diphenhydramine hydrochloride 25 mg/1, ibuprofen 200 mg/1

Manufacturer

TARGET Corporation

Identifiers & Regulatory

Product NDC 11673-225

Product ID 11673-225_46176e6c-0de7-6461-e063-6294a90a9105

Product Type HUMAN OTC DRUG

Marketing Category ANDA

Application Number ANDA090397

Listing Expiration 2026-12-31

Marketing Start 2019-10-30

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 11673225

Hyphenated Format 11673-225

Supplemental Identifiers

RxCUI

901814

UNII

TC2D6JAD40 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, diphenhydramine hcl (source: ndc)

Generic Name ibuprofen, diphenhydramine hcl (source: ndc)

Application Number ANDA090397 (source: ndc)

Routes

ORAL

source: ndc

Resolved Composition

Strengths

25 mg/1
200 mg/1

source: ndc

Packaging

1 BOTTLE in 1 CARTON (11673-225-15) / 40 CAPSULE, LIQUID FILLED in 1 BOTTLE

source: ndc

Packages (1)

11673-225-15 1 BOTTLE in 1 CARTON (11673-225-15) / 40 CAPSULE, LIQUID FILLED in 1 BOTTLE

Ingredients (2)

diphenhydramine hydrochloride (25 mg/1) ibuprofen (200 mg/1)

Linked Drug Pages (1)

IBUPROFEN, DIPHENHYDRAMINE HCL ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload

{"route": ["ORAL"], "spl_id": "46176e6c-0de7-6461-e063-6294a90a9105", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "unii": ["TC2D6JAD40", "WK2XYI10QM"], "rxcui": ["901814"], "spl_set_id": ["97e2c008-1711-dcba-e053-2995a90aa2ff"], "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": ["TARGET Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (11673-225-15)  / 40 CAPSULE, LIQUID FILLED in 1 BOTTLE", "package_ndc": "11673-225-15", "marketing_start_date": "20191030"}], "brand_name": "IBUPROFEN, DIPHENHYDRAMINE HCL", "product_id": "11673-225_46176e6c-0de7-6461-e063-6294a90a9105", "dosage_form": "CAPSULE, LIQUID FILLED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "11673-225", "generic_name": "IBUPROFEN, DIPHENHYDRAMINE HCL", "labeler_name": "TARGET Corporation", "product_type": "HUMAN OTC DRUG", "brand_name_base": "IBUPROFEN, DIPHENHYDRAMINE HCL", "active_ingredients": [{"name": "DIPHENHYDRAMINE HYDROCHLORIDE", "strength": "25 mg/1"}, {"name": "IBUPROFEN", "strength": "200 mg/1"}], "application_number": "ANDA090397", "marketing_category": "ANDA", "marketing_start_date": "20191030", "listing_expiration_date": "20261231"}